ClinVar Genomic variation as it relates to human health
NC_000007.13:g.(?_107002458)_(107204434_?)del
Germline
Classification
(1)
Pathogenic
criteria provided, single submitter
Somatic
No data submitted for somatic clinical impact
Somatic
No data submitted for oncogenicity
Genes
Gene | OMIM | ClinGen Gene Dosage Sensitivity Curation | Variation Viewer | Related variants | ||
---|---|---|---|---|---|---|
HI score | TS score | Within gene | All | |||
COG5 | - | - |
GRCh38 GRCh38 GRCh37 |
776 | 904 | |
DUS4L | - | - | - |
GRCh38 GRCh38 GRCh37 |
- | 70 |
GPR22 | - | - |
GRCh38 GRCh38 GRCh37 |
- | 40 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Pathogenic (1) |
|
Aug 2, 2021 | RCV001983028.5 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Sep 29, 2024