ClinVar Genomic variation as it relates to human health
GRCh37/hg19 7q11.21(chr7:62508852-64940346)x1
Germline
Classification
(1)
Uncertain significance
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 | |||
ERV3-1 | - | - |
GRCh38 GRCh37 |
- | 22 | |
ZNF107 | - | - |
GRCh38 GRCh37 |
55 | 75 | |
ZNF117 | - | - |
GRCh38 GRCh37 |
- | 53 | |
ZNF138 | - | - |
GRCh38 GRCh37 |
23 | 43 | |
ZNF273 | - | - |
GRCh38 GRCh37 |
39 | 60 | |
ZNF679 | - | - | - |
GRCh38 GRCh37 |
38 | 57 |
ZNF680 | - | - | - |
GRCh38 GRCh37 |
28 | 46 |
ZNF727 | - | - | - |
GRCh38 GRCh37 |
41 | 59 |
ZNF735 | - | - | - |
GRCh38 GRCh37 |
34 | 53 |
ZNF736 | - | - | - |
GRCh38 GRCh37 |
25 | 44 |
There is 1 more gene affected by this variant. See the full set of genes in Variation Viewer (GRCh37).
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Nov 20, 2019 | RCV001259999.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Mar 26, 2023