ClinVar Genomic variation as it relates to human health
GRCh38/hg38 16q12.1(chr16:51647991-52422170)x3
Germline
Classification
(1)
Likely benign
no assertion criteria provided
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 | |||
CASC22 | - | - | - | GRCh38 | - | 12 |
LINC00919 | - | - | - | GRCh38 | - | 12 |
LINC01571 | - | - | - | GRCh38 | - | 14 |
LINC02180 | - | - | - | GRCh38 | - | 12 |
LINC02911 | - | - | - |
GRCh38 GRCh37 |
- | 22 |
LOC110120582 | - | - | - | GRCh38 | - | 13 |
LOC110120840 | - | - | - | GRCh38 | - | 10 |
LOC126862348 | - | - | - | GRCh38 | - | 12 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Likely benign (1) |
|
Aug 5, 2011 | RCV000134150.6 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024