ScopeMVZ der Universitätsmedizin Mainz GmbH Humangenetische Praxis Am Fort Mariaborn
110 capabilities
Accredited since July 2025
Verified Oct 2026
One of 3,209 in Germany
Send one structured enquiry and we chase the reply for you. No cold email, no chasing.
Details
Am Fort Mariaborn 1
Mainz 55131 , Germany
Mainz 55131 , Germany
Accreditation
Active
DAkkS
D-ML-21458-01-01
Focuses on cytogenetic analysis and chromosomal assessment for inherited and acquired genetic disorders using techniques such as conventional karyotyping and array-based methods on blood, tissue, and bone marrow samples.
Accreditation Details
Accreditation Body
DAkkS
Number
D-ML-21458-01-01
Status
ActiveSince
21 July 2025
Accreditation is granted under EU Regulation 765/2008 and assessed against ISO/IEC 17025. Data sourced from official DAkkS records.
Download Scope PDFAdditional scope documents
Test Capabilities (110)
| Standard Reference | Description | Category |
|---|---|---|
| Angeborener Chromosomensatz | angeborener Chromosomensatz | Biocompatibility (ISO 10993) |
| (15q11.2)/ PML (15q22-24) | (15q11.2)/ PML (15q22-24) | Molecular Diagnostics / PCR |
| (22q13) Deletion, Rearrangement, DiGeorge-Syndrom | (22q13) Deletion, Rearrangement, DiGeorge-Syndrom | Molecular Diagnostics / PCR |
| 13/18/21, Monosomie 13/18/21, Rearrangement, Paetau-, Edwards-, Down-Syndrom, Aneuploidie der Geschlechtschromosomen | 13/18/21, Monosomie 13/18/21, Rearrangement, Paetau-, Edwards-, Down-Syndrom, Aneuploidie der Geschlechtschromosomen | Molecular Diagnostics / PCR |
| ABL1 (9q34.1)/BCR( 22q11.2) | ABL1 (9q34.1)/BCR( 22q11.2) | Molecular Diagnostics / PCR |
| AML | Deletion, Rearrangement, MDS, AML | Molecular Diagnostics / PCR |
| API2(11q21 )/MALT1(18q21) | API2(11q21 )/MALT1(18q21) | Molecular Diagnostics / PCR |
| ATM (11q22.3)/11 cen (11p11.11- q11) Monosomie 11, Trisomie 11, Rearrangement, CLL | ATM (11q22.3)/11 cen (11p11.11- q11) Monosomie 11, Trisomie 11, Rearrangement, CLL | Molecular Diagnostics / PCR |
| ATM (11q22.3)/TP53(17p13.1) | ATM (11q22.3)/TP53(17p13.1) | Molecular Diagnostics / PCR |
| Acro-p p-Arm: 13,14,15,21,22 | Acro-p p-Arm: 13,14,15,21,22 | Molecular Diagnostics / PCR |
| Amplifikation, Rearrangement | Amplifikation, Rearrangement | Molecular Diagnostics / PCR |
| CBFB (16p21-22) Inversion, Rearrangement, AML | CBFB (16p21-22) Inversion, Rearrangement, AML | Molecular Diagnostics / PCR |
| CDKN2A/ DKN2B ( 9p21 )/CEP 9 | CDKN2A/ DKN2B ( 9p21 )/CEP 9 | Molecular Diagnostics / PCR |
| CLL | Rearrangement, MM, NHL, MCL, CLL | Molecular Diagnostics / PCR |
| D12Z3 (12p11.1-q11) Trisomie 12, Monosomie 12, Rearrangement | D12Z3 (12p11.1-q11) Trisomie 12, Monosomie 12, Rearrangement | Molecular Diagnostics / PCR |
| D15Z1 (15p11.1-q11.1) Trisomie 15, Monosomie 15, Rearrangement | D15Z1 (15p11.1-q11.1) Trisomie 15, Monosomie 15, Rearrangement | Molecular Diagnostics / PCR |
| D18Z1 (18p11-1-q11.1) Trisomie 18, Monosomie 18, Rearrangement | D18Z1 (18p11-1-q11.1) Trisomie 18, Monosomie 18, Rearrangement | Molecular Diagnostics / PCR |
| D20S108 (20q12) Monosomie 20 , Trisomie 20, Rearrangement, AML, MDS | D20S108 (20q12) Monosomie 20 , Trisomie 20, Rearrangement, AML, MDS | Molecular Diagnostics / PCR |
| D20S108(20q12) /20qter(20q13.3) | D20S108(20q12) /20qter(20q13.3) | Molecular Diagnostics / PCR |
| D20Z1(20p11.1-q11.1 ) Trisomie 20, Monosomie 20, Rearrangement | D20Z1(20p11.1-q11.1 ) Trisomie 20, Monosomie 20, Rearrangement | Molecular Diagnostics / PCR |
| D22S75 (N25) (22q11.2)/ARSA | D22S75 (N25) (22q11.2)/ARSA | Molecular Diagnostics / PCR |
| D22S942(HIRA) (22q11)/ARSA | D22S942(HIRA) (22q11)/ARSA | Molecular Diagnostics / PCR |
| D2Z1 2p11.1-q11.1 Trisomie 2, Monosomie 2, Rearrangement | D2Z1 2p11.1-q11.1 Trisomie 2, Monosomie 2, Rearrangement | Molecular Diagnostics / PCR |
| D6Z1 (6p11.1-q11) Trisomie 6, Monosomie 6, Rearrangement | D6Z1 (6p11.1-q11) Trisomie 6, Monosomie 6, Rearrangement | Molecular Diagnostics / PCR |
| D7S486/D7S522 (7q31) Deletion, Rearrangement, Williams-Syndrom | D7S486/D7S522 (7q31) Deletion, Rearrangement, Williams-Syndrom | Molecular Diagnostics / PCR |
| D7Z1 (7p11.1-q11.1 ) Trisomie 7, Monosomie 7, Rearrangement | D7Z1 (7p11.1-q11.1 ) Trisomie 7, Monosomie 7, Rearrangement | Molecular Diagnostics / PCR |
| D8S2291/FGFR1 / D8S1416E (8p11.2) Rerrangement, CML, MPN, Eosinophilie | D8S2291/FGFR1 / D8S1416E (8p11.2) Rerrangement, CML, MPN, Eosinophilie | Molecular Diagnostics / PCR |
| DEK (6p22.3)/LAMC3/NUP214(9q34.1) | DEK (6p22.3)/LAMC3/NUP214(9q34.1) | Molecular Diagnostics / PCR |
| DGCR2 (10p14 )/D10Z1 (10p11.1- q11.1) Deletion,Rearrangement, DiGeorge-Syndrom | DGCR2 (10p14 )/D10Z1 (10p11.1- q11.1) Deletion,Rearrangement, DiGeorge-Syndrom | Molecular Diagnostics / PCR |
| DLEU1 (13q14.2)/ LAMP1 (13q34) | DLEU1 (13q14.2)/ LAMP1 (13q34) | Molecular Diagnostics / PCR |
| DSCR4 (21q22) Trisomie 13/18/21, Monosomie 13/ 18/21, Rearrangement, Paetau-, Edwards-, Down-Syndrom | DSCR4 (21q22) Trisomie 13/18/21, Monosomie 13/ 18/21, Rearrangement, Paetau-, Edwards-, Down-Syndrom | Molecular Diagnostics / PCR |
| DXZ1 (Xp11.1-q11.1)/DYZ3 (Yp11.1- q11.1)/D18Z1( 18p11.1-q11.1 )/RB1 (13q14)/DSCR4 (21q22) Trisomie | DXZ1 (Xp11.1-q11.1)/DYZ3 (Yp11.1- q11.1)/D18Z1( 18p11.1-q11.1 )/RB1 (13q14)/DSCR4 (21q22) Trisomie | Molecular Diagnostics / PCR |
| DXZ1(Xp11.1-q11.1) Monosomie X, Trisomie X, Rearrangement, Turner- Syndrom, Triplo X-Syndrom | DXZ1(Xp11.1-q11.1) Monosomie X, Trisomie X, Rearrangement, Turner- Syndrom, Triplo X-Syndrom | Molecular Diagnostics / PCR |
| DYZ1(Yq12), Aneuploidie des Y- Chomosomes, Rearrangement | DYZ1(Yq12), Aneuploidie des Y- Chomosomes, Rearrangement | Molecular Diagnostics / PCR |
| Deletion, Rearrangement, ALL, CLL, NHL | Deletion, Rearrangement, ALL, CLL, NHL | Molecular Diagnostics / PCR |
| Deletion, Rearrangement, Kallmann- Syndrom | Deletion, Rearrangement, Kallmann- Syndrom | Molecular Diagnostics / PCR |
| Deletion, Rearrangement, Kleinwuchs | Deletion, Rearrangement, Kleinwuchs | Molecular Diagnostics / PCR |
| Deletion, Rearrangement, MDS, MPS | Deletion, Rearrangement, MDS, MPS | Molecular Diagnostics / PCR |
| Deletion, Rearrangement, MM, AML, CML | Deletion, Rearrangement, MM, AML, CML | Molecular Diagnostics / PCR |
| Deletion, Rearrangement, MM, CLL, CML | Deletion, Rearrangement, MM, CLL, CML | Molecular Diagnostics / PCR |
| Deletion, Rearrangement, Prader- Willi-/ Angelmann- Syndrom | Deletion, Rearrangement, Prader- Willi-/ Angelmann- Syndrom | Molecular Diagnostics / PCR |
| Deletion, Rearrangement, Smith- Magenis-Syndrom | Deletion, Rearrangement, Smith- Magenis-Syndrom | Molecular Diagnostics / PCR |
| Deletion, Rearrangement, Steroid | Deletion, Rearrangement, Steroid | Molecular Diagnostics / PCR |
| Deletion, Rearrangement, von Recklinghausen | Deletion, Rearrangement, von Recklinghausen | Molecular Diagnostics / PCR |
| Deletion, Trisomie 9, Monosomie 9, Rearrangement, t-ALL | Deletion, Trisomie 9, Monosomie 9, Rearrangement, t-ALL | Molecular Diagnostics / PCR |
| Deletion,Rearrangement, Miller- Dieker-Syndrom | Deletion,Rearrangement, Miller- Dieker-Syndrom | Molecular Diagnostics / PCR |
| EGFR(7p11)/D7Z1 (7p11.1-q11.1 ) | EGFR(7p11)/D7Z1 (7p11.1-q11.1 ) | Molecular Diagnostics / PCR |
| EGR1 (5q31.2)/RPS14 (5q33.1)/D5S1976 / D5S1518e (5p15.2-15.3) Deletion, Rearrangement, MDS, AML, MM | EGR1 (5q31.2)/RPS14 (5q33.1)/D5S1976 / D5S1518e (5p15.2-15.3) Deletion, Rearrangement, MDS, AML, MM | Molecular Diagnostics / PCR |
| ELN/LIMK1/EIF4H (7q11.23) / | ELN/LIMK1/EIF4H (7q11.23) | Molecular Diagnostics / PCR |
| ETV6 (12p13.2)/RUNX1 ( 21q22.1) | ETV6 (12p13.2)/RUNX1 ( 21q22.1) | Molecular Diagnostics / PCR |
| Geschlechtschromosomenbestimm | Geschlechtschromosomenbestimm | Molecular Diagnostics / PCR |
| IGH (14q32) Rearrangement, MM, NHL, ALL | IGH (14q32) Rearrangement, MM, NHL, ALL | Molecular Diagnostics / PCR |
| IGH (14q32)/MAFB (D20S53/RH65460)(20q12) | IGH (14q32)/MAFB (D20S53/RH65460)(20q12) | Molecular Diagnostics / PCR |
| IGH (14q32.3)/ BCL2 (18q21.3) | IGH (14q32.3)/ BCL2 (18q21.3) | Molecular Diagnostics / PCR |
| IGH (14q32.3)/ MAF (16q23) | IGH (14q32.3)/ MAF (16q23) | Molecular Diagnostics / PCR |
| KALL (Xp22.3)/DXZ1 (Xp11.1-q11.1) | KALL (Xp22.3)/DXZ1 (Xp11.1-q11.1) | Molecular Diagnostics / PCR |
| KMT2A (11q23.3) Rearrangement, ALL, AML | KMT2A (11q23.3) Rearrangement, ALL, AML | Molecular Diagnostics / PCR |
| KMT2E (7q22 )/MET (7q31.2)/D7Z1 (7p11.1-q11.1) Monosomie, Deletion, Rearrangement, MDS, AML | KMT2E (7q22 )/MET (7q31.2)/D7Z1 (7p11.1-q11.1) Monosomie, Deletion, Rearrangement, MDS, AML | Molecular Diagnostics / PCR |
| KMT2E (7q22)/EZH2 (7q36 ) | KMT2E (7q22)/EZH2 (7q36 ) | Molecular Diagnostics / PCR |
| LSI1 (17p13) /RARA(17q21) | LSI1 (17p13) /RARA(17q21) | Molecular Diagnostics / PCR |
| Lymphome | Rearrangement, Amplifikation, Monosomie 8, Trisomie 8, Lymphome | Molecular Diagnostics / PCR |
| MDS | Rearrangement, AML, MDS | Molecular Diagnostics / PCR |
| MECOM (3q26) Rearrangement , Inversion, MDS, AML | MECOM (3q26) Rearrangement , Inversion, MDS, AML | Molecular Diagnostics / PCR |
| MYC (8q24.21)/ 8cen( 8p11.1- q11.1)/IGH(14q32.2) | MYC (8q24.21)/ 8cen( 8p11.1- q11.1)/IGH(14q32.2) | Molecular Diagnostics / PCR |
| MYEOV (11q13.3)/ IGH(14q32.3) | MYEOV (11q13.3)/ IGH(14q32.3) | Molecular Diagnostics / PCR |
| Markerdiagnostik, Rearrangement | Markerdiagnostik, Rearrangement | Molecular Diagnostics / PCR |
| Molekularzytogenetische Analyse nach Mikrodissektion | Molekularzytogenetische Analyse nach Mikrodissektion | Molecular Diagnostics / PCR |
| NF1(17q11.2)/MPO (17q22) | NF1(17q11.2)/MPO (17q22) | Molecular Diagnostics / PCR |
| NUP 98 (11p15.4) Rearrangement, AML | NUP 98 (11p15.4) Rearrangement, AML | Molecular Diagnostics / PCR |
| PML (15q24)/RARA(17q21.1-21.2) | PML (15q24)/RARA(17q21.1-21.2) | Molecular Diagnostics / PCR |
| PN 21 /RCAN (21q22) Trisomie 21, Monsomie 21, Rearrangement, Down-Syndrom | PN 21 /RCAN (21q22) Trisomie 21, Monsomie 21, Rearrangement, Down-Syndrom | Molecular Diagnostics / PCR |
| RB1(13q14)/MALT1 (18q21) / | RB1 (13q14)/MALT1 (18q21) | Molecular Diagnostics / PCR |
| RUNX1T1(8q21.3- 22.1)/RUNX1(21q22.1) | RUNX1T1(8q21.3- 22.1)/RUNX1(21q22.1) | Molecular Diagnostics / PCR |
| Rearrangement, ALL | Rearrangement, ALL | Molecular Diagnostics / PCR |
| Rearrangement, AML | Rearrangement, AML | Molecular Diagnostics / PCR |
| Rearrangement, CLL | Rearrangement, CLL | Molecular Diagnostics / PCR |
| Rearrangement, CML | Rearrangement, CML | Molecular Diagnostics / PCR |
| Rearrangement, MM | Rearrangement, MM | Molecular Diagnostics / PCR |
| Rearrangement, NHL, DLBCL | Rearrangement, NHL, DLBCL | Molecular Diagnostics / PCR |
| SEC63 (6q21)/MYB (6q23.3) | SEC63 (6q21)/MYB (6q23.3) | Molecular Diagnostics / PCR |
| SHOX (Xp22)/DXZ1 (Xp11.1-q11.1) | SHOX (Xp22)/DXZ1 (Xp11.1-q11.1) | Molecular Diagnostics / PCR |
| SMS (17p11.2)/RARA(17q21.1) | SMS (17p11.2)/RARA(17q21.1) | Molecular Diagnostics / PCR |
| SNRPN/UBE3A (15q11-13)/D15Z1 | SNRPN/UBE3A (15q11-13)/D15Z1 | Molecular Diagnostics / PCR |
| SRY (Yp11.3) Deletion, Rearrangement | SRY (Yp11.3) Deletion, Rearrangement | Molecular Diagnostics / PCR |
| STS (Xp22.3)/DXZ1 (Xp11.1-q11.1) | STS (Xp22.3)/DXZ1 (Xp11.1-q11.1) | Molecular Diagnostics / PCR |
| Sulfatase-Mangel | Sulfatase-Mangel | Molecular Diagnostics / PCR |
| Syndrom, XXY-Syndrom,Triplo X- Syndrom | Syndrom, XXY-Syndrom,Triplo X- Syndrom | Molecular Diagnostics / PCR |
| TCRAD (14q11.2) Rearrangement, ALL, NHL | TCRAD (14q11.2) Rearrangement, ALL, NHL | Molecular Diagnostics / PCR |
| TP53 (17p13 )/NF1(17q11.2) | TP53 (17p13 )/NF1(17q11.2) | Molecular Diagnostics / PCR |
| Telomer 1-22 /X/Y p-Arm und q- Arm Rearrangement Chromosom 1- 22 | Telomer 1-22 /X/Y p-Arm und q- Arm Rearrangement Chromosom 1- 22 | Molecular Diagnostics / PCR |
| X (Xp11.1-q11.1)/Y(Yp11.1-q11.1) | X (Xp11.1-q11.1)/Y(Yp11.1-q11.1) | Molecular Diagnostics / PCR |
| XIST/CHIC1 (Xq13)/DXZ1 (Xp11.1- q11.1) Deletion, Rearrangement, X- Inaktivierung | XIST/CHIC1 (Xq13)/DXZ1 (Xp11.1- q11.1) Deletion, Rearrangement, X- Inaktivierung | Molecular Diagnostics / PCR |
| ung, Turner-Syndrom, Klinefelter | ung, Turner-Syndrom, Klinefelter | Molecular Diagnostics / PCR |
| a Die Proben werden vom Labor ohne vorherige histologische Beurteilung | a Die Proben werden vom Labor ohne vorherige histologische Beurteilung | Other |
| (5p15.2) Deletion, Rearrangement, Cri-du-chat- Syndrom | (5p15.2) Deletion, Rearrangement, Cri-du-chat- Syndrom | Sterility Testing |
| ALK (2p23) D2S2312 (2p23) | ALK (2p23) D2S2312 (2p23) | Sterility Testing |
| Amplifikation, Deletion, Rearrangement, MM | Amplifikation, Deletion, Rearrangement, MM | Sterility Testing |
| BCL6 3q27 Rearrangement, NHL | BCL6 3q27 Rearrangement, NHL | Sterility Testing |
| CDKN2C(1p32.3 )/CKS1B ( 1q21-22) | CDKN2C(1p32.3 )/CKS1B ( 1q21-22) | Sterility Testing |
| Deletion 4p16.3, Rearrangement, Wolf-Hirschhorn Syndrom | Deletion 4p16.3, Rearrangement, Wolf-Hirschhorn Syndrom | Sterility Testing |
| Deletion, Rearrangement, CML, MPN, Eosinophilie | Deletion, Rearrangement, CML, MPN, Eosinophilie | Sterility Testing |
| FGFR3 (4p16.3)/IGH(14q32.3) | FGFR3 (4p16.3)/IGH(14q32.3) | Sterility Testing |
| NSD1 (5q35)/D5S721/D5S23 | NSD1 (5q35)/D5S721/D5S23 | Sterility Testing |
| NSD2 (4p16.3 4)/(4p11-q11) | NSD2 (4p16.3 4)/(4p11-q11) | Sterility Testing |
| PDGFRB (5q32) 5q32 | PDGFRB (5q32) 5q32 | Sterility Testing |
| Rearrangement, CML, atyp. CML | Rearrangement, CML, atyp. CML | Sterility Testing |
| Rearrangement, NHL | Rearrangement, NHL | Sterility Testing |
| Rearrangement, prä B-AML | Rearrangement, prä B-AML | Sterility Testing |
| SCFD2/CHIC2 LNX1/PDGFRA (4q12) | SCFD2/CHIC2 LNX1/PDGFRA (4q12) | Sterility Testing |
| TCF3(11q23)/PBX(11q23)(19p13.3) | TCF3(11q23)/PBX(11q23)(19p13.3) | Sterility Testing |
Send an Enquiry
Request a quote, ask about capacity, or discuss your testing requirements directly with this lab.