ClinVar Genomic variation as it relates to human health
GRCh38/hg38 10q11.22(chr10:46146977-46737090)x1
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 | |||
ANTXRL | - | - | - | GRCh38 | - | 55 |
ANXA8L1 | - | - | - |
GRCh38 GRCh37 |
10 | 120 |
GPRIN2 | - | - |
GRCh38 GRCh38 GRCh37 |
19 | 133 | |
LINC00842 | - | - | - | GRCh38 | - | 59 |
LINC02637 | - | - | - | GRCh38 | - | 66 |
LOC105378289 | - | - | - | GRCh38 | - | 66 |
LOC105378577 | - | - | - | GRCh38 | - | 55 |
LOC111818966 | - | - | - | GRCh38 | - | 67 |
LOC130003769 | - | - | - | GRCh38 | 1 | 57 |
LOC130003770 | - | - | - | GRCh38 | - | 56 |
There are 4 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 |
---|---|---|---|---|
See cases
|
Benign (1) |
|
Sep 21, 2012 | RCV000138474.6 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024