ClinVar Genomic variation as it relates to human health
GRCh37/hg19 6p25.1-22.3(chr6:5354402-17950079)x1
Germline
Classification
(1)
Pathogenic
criteria provided, single submitter
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 | |||
DSP | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
4694 | 4907 | |
NEDD9 | Little evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
39 | 78 | |
JARID2 | No evidence available | No evidence available |
GRCh38 GRCh37 |
177 | 210 | |
ADTRP | - | - |
GRCh38 GRCh37 |
11 | 39 | |
ATXN1 | - | - |
GRCh38 GRCh37 |
86 | 144 | |
BLOC1S5 | - | - |
GRCh38 GRCh37 |
2 | 55 | |
BMP6 | - | - |
GRCh38 GRCh37 |
69 | 103 | |
C6orf52 | - | - | - |
GRCh38 GRCh38 GRCh37 |
2 | 40 |
CAGE1 | - | - |
GRCh38 GRCh37 |
38 | 84 | |
CAP2 | - | - |
GRCh38 GRCh37 |
28 | 55 |
There are 43 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 |
---|---|---|---|---|
Pathogenic (1) |
|
Jan 20, 2016 | RCV000240576.2 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Oct 15, 2023