ClinVar Genomic variation as it relates to human health
GRCh38/hg38 10p13(chr10:15569469-16776796)x3
Germline
Classification
(1)
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 | |||
C1QL3 | - | - |
GRCh38 GRCh37 |
5 | 30 | |
ITGA8 | - | - |
GRCh38 GRCh37 |
303 | 327 | |
LINC02654 | - | - | - | GRCh38 | - | 9 |
LOC111946223 | - | - | - | GRCh38 | - | 7 |
LOC111946224 | - | - | - | GRCh38 | - | 7 |
LOC111946225 | - | - | - | GRCh38 | - | 7 |
LOC121366044 | - | - | - | GRCh38 | - | 9 |
LOC129390137 | - | - | - | GRCh38 | - | 8 |
LOC129390138 | - | - | - | GRCh38 | - | 9 |
LOC129390139 | - | - | - | GRCh38 | - | 8 |
There are 14 more genes affected by this variant. See the full set of genes in Variation Viewer (GRCh38 , GRCh37 , NCBI36).
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Benign (1) |
|
Jul 30, 2009 | RCV000135483.5 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024