ClinVar Genomic variation as it relates to human health
GRCh38/hg38 1p13.2(chr1:112625023-113046966)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 | |||
MOV10 | No evidence available | No evidence available |
GRCh38 GRCh37 |
50 | 72 | |
CAPZA1 | - | - |
GRCh38 GRCh37 |
19 | 40 | |
LINC01356 | - | - | - | GRCh38 | - | 6 |
LINC01357 | - | - | - | GRCh38 | - | 6 |
LOC110121184 | - | - | - |
GRCh38 GRCh38 |
- | 5 |
LOC112577477 | - | - | - | GRCh38 | - | 5 |
LOC112577478 | - | - | - | GRCh38 | - | 5 |
LOC113939977 | - | - | - |
GRCh38 GRCh38 |
- | 5 |
LOC120893153 | - | - | - | GRCh38 | - | 15 |
LOC120893154 | - | - | - | GRCh38 | - | 5 |
There are 19 more genes affected by this variant. See the full set of genes in Variation Viewer (GRCh38 , GRCh37 , NCBI36) and ClinGen Dosage Sensitivity Map.
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Likely benign (1) |
|
Oct 30, 2010 | RCV000135999.5 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024