ClinVar Genomic variation as it relates to human health
GRCh37/hg19 15q15.1(chr15:40464942-41196807)x4
Germline
Classification
(1)
Uncertain significance
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 | |||
ANKRD63 | - | - | - |
GRCh38 GRCh37 |
15 | 25 |
BAHD1 | - | - |
GRCh38 GRCh37 |
56 | 65 | |
BUB1B | - | - |
GRCh38 GRCh37 |
1477 | 1746 | |
C15orf62 | - | - | - |
GRCh38 GRCh37 |
- | 11 |
CCDC32 | - | - |
GRCh38 GRCh37 |
8 | 17 | |
CCDC9B | - | - | - |
GRCh38 GRCh37 |
5 | 14 |
CHST14 | - | - |
GRCh38 GRCh37 |
221 | 303 | |
DISP2 | - | - |
GRCh38 GRCh37 |
92 | 111 | |
DNAJC17 | - | - |
GRCh38 GRCh37 |
170 | 197 | |
GCHFR | - | - |
GRCh38 GRCh37 |
- | 12 |
There are 15 more genes affected by this variant. See the full set of genes in Variation Viewer (GRCh37).
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Jun 26, 2019 | RCV001259208.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Apr 25, 2022