Medicover Genetics GmbH (Medicover Humangenetik Berlin-Lichtenberg MVZ), MCG
General information
Medicover Genetics GmbH, MCG
Medicover Humangenetik Berlin-Lichtenberg MVZ
Plauener Strasse 163-165
Berlin
Germany - 13053
https://www.medicover-genetics.de/
Organization ID: 507452
Medicover Humangenetik Berlin-Lichtenberg MVZ
Plauener Strasse 163-165
Berlin
Germany - 13053
https://www.medicover-genetics.de/
Organization ID: 507452
Personnel
- Oriane Vedrines, Variant scientist/curator
Phone: +33650923501
Email: oriane.vedrines@medicover-genetics.de - Markus Stumm, Lab Director
Phone: +493092090744
Email: Markus.Stumm@medicover.de - Oriane Vedrines, Variant scientist/curator
Phone: +33650923501
Email: oriane.vedrines@medicover-genetics.de - Andre Weber, Variant scientist/curator
Phone: +493092090744
Email: andre.weber@medicover-genetics.de
Assertion criteria
Level: Assertion criteria not provided
Summary of submissions to ClinVar
Total submissions: 58
Condition
| Name | Submissions | Last Updated |
|---|---|---|
| 10q11.22q11.23 microdeletion including CHAT and SLC18A3 | 1 | Sep 8, 2020 |
| 13q12.2q12.3 deletion | 1 | Aug 23, 2021 |
| 14q11.2 microduplication | 1 | Nov 23, 2021 |
| 14q22.2q24.3 duplication | 1 | Jun 3, 2021 |
| 16p11.2 duplication syndrome | 1 | Jan 3, 2022 |
| 1p36.1 deletion syndrome | 1 | Sep 1, 2021 |
| 2p24.1p23.3 microdeletion syndrome | 1 | Apr 14, 2023 |
| 2q13q22.3 microduplication syndrome | 1 | Apr 28, 2022 |
| 3p- syndrome | 1 | Sep 27, 2023 |
| 3q28q29 deletion syndrome | 1 | Nov 23, 2021 |
| 7p21.3p21.2 microduplication | 1 | Nov 9, 2021 |
| 9p23 dn microdeletion | 1 | Aug 23, 2021 |
| Autism, susceptibility to, X-linked 4 | 1 | Sep 13, 2023 |
| Chromosome 15q13.3 microdeletion syndrome | 1 | Apr 4, 2023 |
| Chromosome 16p12.2-p11.2 deletion syndrome | 1 | Jul 20, 2023 |
| Chromosome 2q32-q33 deletion syndrome | 1 | Aug 31, 2020 |
| Chromosome 3q13.31 deletion syndrome | 2 | Apr 14, 2023 |
| Chromosome 5p13 duplication syndrome | 1 | Apr 13, 2023 |
| Complex neurodevelopmental disorder | 1 | Feb 3, 2022 |
| Deletion of long arm of chromosome 18 | 1 | May 3, 2023 |
| Imagawa-Matsumoto syndrome | 1 | Oct 6, 2020 |
| Intellectual developmental disorder with autism and macrocephaly | 1 | Jun 30, 2020 |
| Intellectual developmental disorder, autosomal dominant 63, with macrocephaly | 1 | May 15, 2023 |
| Intellectual disability, X-linked, with or without seizures, arx-related | 1 | Dec 19, 2023 |
| Lynch syndrome 1 | 2 | May 30, 2023 |
| Motor developmental delay due to 14q32.2 paternally expressed gene defect | 1 | Sep 29, 2023 |
| Nanophthalmos 4 | 1 | Oct 6, 2020 |
| Proximal 16p11.2 microdeletion syndrome | 1 | Aug 18, 2023 |
| See cases | 24 | Jan 29, 2024 |
| Xq21.32q23 deletion | 1 | Aug 23, 2021 |
| del2p16.3 | 1 | Apr 29, 2022 |
| del3q29 | 1 | Aug 31, 2021 |
| duplication 8q12 | 1 | Jul 15, 2020 |
| microdeletion 4p16.3p16.1 | 1 | Jul 9, 2020 |
| mircrodeletion 17q11.2q12 including TMEM98 and SUZ12 | 1 | Oct 6, 2020 |