Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Institute of Human Genetics, |
RCV003329513 | SCV004036099 | pathogenic | Velocardiofacial syndrome | 2022-06-20 | criteria provided, single submitter | clinical testing | |
Institute of Human Genetics, |
RCV003329514 | SCV004036115 | pathogenic | Chromosome 22q11.2 deletion syndrome, distal | 2022-11-23 | criteria provided, single submitter | clinical testing |