ClinVar Genomic variation as it relates to human health
GRCh38/hg38 7q11.21(chr7:63868094-64494908)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 | |||
LINC01005 | - | - | - | GRCh38 | - | 7 |
LINC02848 | - | - | - | GRCh38 | - | 7 |
LOC129389798 | - | - | - | GRCh38 | - | 7 |
LOC129998503 | - | - | - | GRCh38 | - | 7 |
LOC129998504 | - | - | - | GRCh38 | - | 7 |
LOC129998505 | - | - | - | GRCh38 | - | 7 |
LOC129998506 | - | - | - | GRCh38 | - | 7 |
ZNF679 | - | - | - |
GRCh38 GRCh37 |
42 | 61 |
ZNF722 | - | - | - | GRCh38 | - | 7 |
ZNF727 | - | - | - |
GRCh38 GRCh37 |
52 | 70 |
There are 2 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) |
|
Oct 19, 2010 | RCV000136973.5 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024