ClinVar Genomic variation as it relates to human health
GRCh37/hg19 7q11.21(chr7:62495083-64927758)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 |
48 | 68 | |
ZNF117 | - | - |
GRCh38 GRCh37 |
- | 47 | |
ZNF138 | - | - |
GRCh38 GRCh37 |
21 | 41 | |
ZNF273 | - | - |
GRCh38 GRCh37 |
28 | 49 | |
ZNF679 | - | - | - |
GRCh38 GRCh37 |
32 | 51 |
ZNF680 | - | - | - |
GRCh38 GRCh37 |
22 | 40 |
ZNF727 | - | - | - |
GRCh38 GRCh37 |
38 | 56 |
ZNF735 | - | - | - |
GRCh38 GRCh37 |
32 | 51 |
ZNF736 | - | - | - |
GRCh38 GRCh37 |
22 | 41 |
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) |
|
Jul 18, 2018 | RCV001263023.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Mar 26, 2023