ClinVar Genomic variation as it relates to human health
GRCh37/hg19 6p22.1(chr6:27616157-28011557)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 | |||
H1-5 | - | - |
GRCh38 GRCh37 |
22 | 36 | |
H2AC13 | - | - |
GRCh38 GRCh37 |
5 | 13 | |
H2AC14 | - | - |
GRCh38 GRCh37 |
6 | 14 | |
H2AC15 | - | - |
GRCh38 GRCh37 |
8 | 24 | |
H2AC16 | - | - |
GRCh38 GRCh37 |
10 | 18 | |
H2AC17 | - | - |
GRCh38 GRCh37 |
11 | 19 | |
H2BC13 | - | - |
GRCh38 GRCh37 |
3 | 11 | |
H2BC14 | - | - |
GRCh38 GRCh37 |
7 | 15 | |
H2BC15 | - | - |
GRCh38 GRCh37 |
2 | 12 | |
H2BC17 | - | - |
GRCh38 GRCh37 |
2 | 15 |
There are 9 more genes 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 |
---|---|---|---|---|
Likely benign (1) |
|
Apr 1, 2019 | RCV001005790.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Apr 25, 2022