ClinVar Genomic variation as it relates to human health
GRCh38/hg38 7q11.21(chr7:65017875-65835330)x1
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 | |||
LINC03006 | - | - | - | GRCh38 | - | 9 |
LOC123956154 | - | - | - | GRCh38 | - | 9 |
LOC129389801 | - | - | - | GRCh38 | - | 9 |
LOC129389802 | - | - | - | GRCh38 | - | 11 |
LOC129389803 | - | - | - | GRCh38 | - | 14 |
LOC129998515 | - | - | - | GRCh38 | - | 9 |
LOC129998516 | - | - | - | GRCh38 | - | 9 |
LOC129998517 | - | - | - | GRCh38 | - | 9 |
LOC129998518 | - | - | - | GRCh38 | - | 9 |
LOC129998519 | - | - | - | GRCh38 | - | 9 |
There are 6 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) |
|
Oct 10, 2011 | RCV000139720.5 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024