ClinVar Genomic variation as it relates to human health
GRCh38/hg38 6p22.2(chr6:25991391-26116829)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 | |||
H1-1 | - | - |
GRCh38 GRCh37 |
38 | 50 | |
H1-2 | - | - |
GRCh38 GRCh37 |
27 | 77 | |
H1-6 | - | - |
GRCh38 GRCh37 |
41 | 58 | |
H2AC4 | - | - |
GRCh38 GRCh37 |
17 | 30 | |
H2BC3 | - | - |
GRCh38 GRCh37 |
15 | 28 | |
H2BC4 | - | - |
GRCh38 GRCh37 |
- | 23 | |
H3C1 | - | - |
GRCh38 GRCh37 |
24 | 37 | |
H3C2 | - | - |
GRCh38 GRCh37 |
2 | 22 | |
H3C3 | - | - |
GRCh38 GRCh37 |
2 | 21 | |
H4C1 | - | - |
GRCh38 GRCh37 |
6 | 19 |
There are 22 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
|
Likely benign (1) |
|
Apr 30, 2011 | RCV000140950.3 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Oct 15, 2023