ClinVar Genomic variation as it relates to human health
GRCh38/hg38 6p22.2(chr6:25991402-26280693)x3
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 | |||
H1-4 | No evidence available | No evidence available |
GRCh38 GRCh37 |
110 | 126 | |
H1-1 | - | - |
GRCh38 GRCh37 |
10 | 22 | |
H1-2 | - | - |
GRCh38 GRCh37 |
6 | 30 | |
H1-3 | - | - |
GRCh38 GRCh37 |
17 | 31 | |
H1-6 | - | - |
GRCh38 GRCh37 |
17 | 34 | |
H2AC4 | - | - |
GRCh38 GRCh37 |
9 | 22 | |
H2AC6 | - | - |
GRCh38 GRCh37 |
- | 18 | |
H2AC7 | - | - |
GRCh38 GRCh37 |
- | 19 | |
H2AC8 | - | - |
GRCh38 GRCh37 |
- | 14 | |
H2BC10 | - | - |
GRCh38 GRCh37 |
- | 21 |
There are 77 more genes affected by this variant. See the full set of genes in Variation Viewer (GRCh38 , GRCh37 , NCBI36) and ClinGen Dosage Sensitivity Map.
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Likely benign (1) |
|
Sep 21, 2012 | RCV000139521.4 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Oct 15, 2023