ClinVar Genomic variation as it relates to human health
GRCh37/hg19 6p22.2(chr6:26104332-26365573)x4
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 | |||
H1-4 | No evidence available | No evidence available |
GRCh38 GRCh37 |
153 | 169 | |
BTN3A2 | - | - |
GRCh38 GRCh37 |
23 | 36 | |
H1-3 | - | - |
GRCh38 GRCh37 |
54 | 68 | |
H1-6 | - | - |
GRCh38 GRCh37 |
41 | 58 | |
H2AC6 | - | - |
GRCh38 GRCh37 |
- | 21 | |
H2AC7 | - | - |
GRCh38 GRCh37 |
- | 29 | |
H2AC8 | - | - |
GRCh38 GRCh37 |
3 | 17 | |
H2BC10 | - | - |
GRCh38 GRCh37 |
- | 27 | |
H2BC4 | - | - |
GRCh38 GRCh37 |
- | 23 | |
H2BC5 | - | - |
GRCh38 GRCh37 |
7 | 23 |
There are 16 more genes affected by this variant. See the full set of genes in Variation Viewer (GRCh37) and ClinGen Dosage Sensitivity Map.
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Jul 20, 2015 | RCV000207323.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Feb 14, 2024