ScopeMVZ der Universitätsmedizin Mainz GmbH Humangenetische Praxis Am Fort Mariaborn
133 capabilities
Accredited since July 2025
Verified Apr 2026
One of 3,039 in Germany
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.
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Test Capabilities (133)
| Standard Reference | Description | Category |
|---|---|---|
| Angeborener Chromosomensatz | angeborener Chromosomensatz | Biocompatibility (ISO 10993) |
| 0,8 0,1 0,22 | 0,8 0,1 0,22 | Electrical |
| (13q14)/DSCR4 (21q22) Trisomie | (13q14)/DSCR4 (21q22) Trisomie | Molecular Diagnostics / PCR |
| (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 |
| (6p22.3)/LAMC3/NUP214(9q34.1) | (6p22.3)/LAMC3/NUP214(9q34.1) | Molecular Diagnostics / PCR |
| (7p11.1-q11.1) Monosomie, Deletion, Rearrangement, MDS, AML | (7p11.1-q11.1) Monosomie, Deletion, Rearrangement, MDS, AML | Molecular Diagnostics / PCR |
| (8p11.2) Rerrangement, CML, MPN, Eosinophilie | (8p11.2) Rerrangement, CML, MPN, Eosinophilie | Molecular Diagnostics / PCR |
| (D20S53/RH65460)(20q12) | (D20S53/RH65460)(20q12) | Molecular Diagnostics / PCR |
| 13/18/21, Monosomie 13/18/21, Rearrangement, Paetau-, Edwards-, Down-Syndrom, Aneuploidie der | 13/18/21, Monosomie 13/18/21, Rearrangement, Paetau-, Edwards-, Down-Syndrom, Aneuploidie der | Molecular Diagnostics / PCR |
| ABL1 (9q34.1)/BCR( 22q11.2) | ABL1 (9q34.1)/BCR( 22q11.2) | Molecular Diagnostics / PCR |
| API2(11q21 )/MALT1(18q21) | API2(11q21 )/MALT1(18q21) | 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 |
| Arm Rearrangement Chromosom | Arm Rearrangement Chromosom | 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 |
| Chomosomes, Rearrangement | Chomosomes, Rearrangement | Molecular Diagnostics / PCR |
| D12Z3 (12p11.1-q11) Trisomie | D12Z3 (12p11.1-q11) Trisomie | Molecular Diagnostics / PCR |
| D15Z1 (15p11.1-q11.1) Trisomie | D15Z1 (15p11.1-q11.1) Trisomie | Molecular Diagnostics / PCR |
| D18Z1 (18p11-1-q11.1) Trisomie | D18Z1 (18p11-1-q11.1) Trisomie | Molecular Diagnostics / PCR |
| D20S108 (20q12) Monosomie 20 | D20S108 (20q12) Monosomie 20 | Molecular Diagnostics / PCR |
| D20S108(20q12) /20qter(20q13.3) | D20S108(20q12) /20qter(20q13.3) | Molecular Diagnostics / PCR |
| D20Z1(20p11.1-q11.1 ) Trisomie | D20Z1(20p11.1-q11.1 ) Trisomie | 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 |
| D7S486/D7S522 (7q31) Deletion, Rearrangement, Williams-Syndrom | D7S486/D7S522 (7q31) Deletion, Rearrangement, Williams-Syndrom | Molecular Diagnostics / PCR |
| D8S2291/FGFR1 / D8S1416E | D8S2291/FGFR1 / D8S1416E | 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) Monosomie | DXZ1(Xp11.1-q11.1) Monosomie | Molecular Diagnostics / PCR |
| Deletion, Rearrangement, ALL, NHL | Deletion, Rearrangement, ALL, NHL | Molecular Diagnostics / PCR |
| Deletion, Rearrangement, Kleinwuchs | Deletion, Rearrangement, Kleinwuchs | Molecular Diagnostics / PCR |
| Deletion, Rearrangement, MDS, AML | Deletion, Rearrangement, MDS, AML | 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, CML | Deletion, Rearrangement, MM, CML | Molecular Diagnostics / PCR |
| Deletion, Rearrangement, Steroid | Deletion, Rearrangement, Steroid | Molecular Diagnostics / PCR |
| Deletion, Rearrangement, von | Deletion, Rearrangement, von | Molecular Diagnostics / PCR |
| Deletion, Trisomie 9, Monosomie | Deletion, Trisomie 9, Monosomie | Molecular Diagnostics / PCR |
| Dieker-Syndrom | Miller-Dieker-Syndrom | 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 |
| Geschlechtschromosomen | Geschlechtschromosomen | Molecular Diagnostics / PCR |
| Geschlechtschromosomenbestimm | Geschlechtschromosomenbestimm | Molecular Diagnostics / PCR |
| Glut1-Defizienz-Syndrom | Glut1-Defizienz-Syndrom | Molecular Diagnostics / PCR |
| IGH (14q32) Rearrangement, MM, NHL, ALL | IGH (14q32) Rearrangement, MM, NHL, ALL | Molecular Diagnostics / PCR |
| IGH (14q32)/MAFB | IGH (14q32)/MAFB | 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 | KMT2E (7q22 )/MET (7q31.2)/D7Z1 | 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 |
| MYEOV (11q13.3)/ IGH(14q32.3) | MYEOV (11q13.3)/ IGH(14q32.3) | Molecular Diagnostics / PCR |
| Magenis-Syndrom | Smith-Magenis-Syndrom | Molecular Diagnostics / PCR |
| Markerdiagnostik, Rearrangement | Markerdiagnostik, Rearrangement | Molecular Diagnostics / PCR |
| Monosomie 12, Rearrangement | Monosomie 12, Rearrangement | Molecular Diagnostics / PCR |
| Monosomie 15, Rearrangement | Monosomie 15, Rearrangement | Molecular Diagnostics / PCR |
| Monosomie 18, Rearrangement | Monosomie 18, Rearrangement | Molecular Diagnostics / PCR |
| Monosomie 20, Rearrangement | Monosomie 20, Rearrangement | Molecular Diagnostics / PCR |
| Monosomie 6, Rearrangement | Monosomie 6, Rearrangement | Molecular Diagnostics / PCR |
| Monosomie 7, Rearrangement | Monosomie 7, Rearrangement | Molecular Diagnostics / PCR |
| Monsomie 21, Rearrangement, Down-Syndrom | Monsomie 21, Rearrangement, Down-Syndrom | 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 | PN 21 /RCAN (21q22) Trisomie | Molecular Diagnostics / PCR |
| Prader-Willi-/Angelmann-Syndrom | Prader-Willi-/Angelmann-Syndrom | Molecular Diagnostics / PCR |
| RB1(13q14)/MALT1 (18q21) / | RB1(13q14)/MALT1 (18q21) / | Molecular Diagnostics / PCR |
| Rearrangement | T-Zellrezeptor Gamma Rearrangement | Molecular Diagnostics / PCR |
| Rearrangement, ALL | Rearrangement, ALL | Molecular Diagnostics / PCR |
| Rearrangement, AML | Rearrangement, AML | Molecular Diagnostics / PCR |
| Rearrangement, AML, MDS | Rearrangement, AML, MDS | Molecular Diagnostics / PCR |
| Rearrangement, Amplifikation, Monosomie 8, Trisomie 8, Lymphome | Rearrangement, Amplifikation, Monosomie 8, Trisomie 8, Lymphome | Molecular Diagnostics / PCR |
| Rearrangement, CML | Rearrangement, CML | Molecular Diagnostics / PCR |
| Rearrangement, MM, NHL, MCL, CLL | Rearrangement, MM, NHL, MCL, CLL | Molecular Diagnostics / PCR |
| Rearrangement, NHL, DLBCL | Rearrangement, NHL, DLBCL | Molecular Diagnostics / PCR |
| Rearrangement, t-ALL | Rearrangement, t-ALL | Molecular Diagnostics / PCR |
| Recklinghausen | Recklinghausen | 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 |
| 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, Triplo X-Syndrom | 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 | Telomer 1-22 /X/Y p-Arm und | Molecular Diagnostics / PCR |
| Trisomie 20, Rearrangement, AML, MDS | Trisomie 20, Rearrangement, AML, MDS | 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 |
| ung, Turner-Syndrom, Klinefelter | ung, Turner-Syndrom, Klinefelter | Molecular Diagnostics / PCR |
| 22.1)/RUNX1(21q22.1) | 22.1)/RUNX1(21q22.1) | Other |
| ATM (11q22.3)/11 cen (11p11.11- | ATM (11q22.3)/11 cen (11p11.11- | Other |
| DEK | DEK | Other |
| DGCR2 (10p14 )/D10Z1 (10p11.1- | DGCR2 (10p14 )/D10Z1 (10p11.1- | Other |
| DXZ1 (Xp11.1-q11.1)/DYZ3 (Yp11.1- | DXZ1 (Xp11.1-q11.1)/DYZ3 (Yp11.1- | Other |
| EGFR(7p11)/D7Z1 (7p11.1-q11.1 | EGFR(7p11)/D7Z1 (7p11.1-q11.1 | Other |
| MYC (8q24.21)/ 8cen( 8p11.1- | MYC (8q24.21)/ 8cen( 8p11.1- | Other |
| RUNX1T1(8q21.3- | RUNX1T1(8q21.3- | Other |
| Rearrangement, CLL | q11) Monosomie 11, Trisomie 11, Rearrangement, CLL | Other |
| XIST/CHIC1 (Xq13)/DXZ1 (Xp11.1- | XIST/CHIC1 (Xq13)/DXZ1 (Xp11.1- | Other |
| q11.1) Deletion, Rearrangement, Inaktivierung | q11.1) Deletion, Rearrangement, Inaktivierung | Other |
| q11.1) Deletion,Rearrangement, DiGeorge-Syndrom | q11.1) Deletion,Rearrangement, DiGeorge-Syndrom | Other |
| q11.1)/D18Z1( 18p11.1-q11.1 )/RB1 | q11.1)/D18Z1( 18p11.1-q11.1 )/RB1 | Other |
| q11.1)/IGH(14q32.2) | q11.1)/IGH(14q32.2) | Other |
| (5p15.2) Deletion, Rearrangement, Cri-du-chat- Syndrom | (5p15.2) Deletion, Rearrangement, Cri-du-chat- Syndrom | Sterility Testing |
| (5p15.2-15.3) Deletion, Rearrangement, MDS, AML, MM | (5p15.2-15.3) Deletion, Rearrangement, MDS, AML, MM | Sterility Testing |
| (5q33.1)/D5S1976 / D5S1518e | (5q33.1)/D5S1976 / D5S1518e | 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 |
| D2Z1 2p11.1-q11.1 Trisomie | D2Z1 2p11.1-q11.1 Trisomie | 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 |
| EGR1 (5q31.2)/RPS14 | EGR1 (5q31.2)/RPS14 | Sterility Testing |
| FGFR3 (4p16.3)/IGH(14q32.3) | FGFR3 (4p16.3)/IGH(14q32.3) | Sterility Testing |
| Inversion, MDS, AML | Inversion, MDS, AML | Sterility Testing |
| MECOM (3q26) Rearrangement | MECOM (3q26) Rearrangement | Sterility Testing |
| Molekularzytogenetische Analyse | Molekularzytogenetische Analyse | Sterility Testing |
| Monosomie 2, Rearrangement | Monosomie 2, Rearrangement | 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 |