ClinVar Genomic variation as it relates to human health
GRCh38/hg38 7q36.3(chr7:158082354-158591823)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 | |||
LINC01022 | - | - | - | GRCh38 | - | 53 |
LOC110599567 | - | - | - | GRCh38 | - | 53 |
LOC113687208 | - | - | - | GRCh38 | - | 53 |
LOC114004407 | - | - | - | GRCh38 | - | 55 |
LOC121740707 | - | - | - | GRCh38 | - | 53 |
LOC126860258 | - | - | - |
GRCh38 GRCh38 |
- | 54 |
LOC126860259 | - | - | - |
GRCh38 GRCh38 |
- | 55 |
LOC129389949 | - | - | - |
GRCh38 GRCh38 |
- | 55 |
LOC129389950 | - | - | - | GRCh38 | - | 55 |
LOC132089520 | - | - | - | GRCh38 | - | 55 |
There are 3 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 |
---|---|---|---|---|
Likely benign (1) |
|
Nov 30, 2010 | RCV000135148.3 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Oct 15, 2023