ClinVar Genomic variation as it relates to human health
GRCh37/hg19 5q35.3(chr5:176643613-179085551)x3
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 | |||
DDX41 | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
530 | 596 | |
NSD1 | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
1674 | 1787 | |
ADAMTS2 | - | - |
GRCh38 GRCh38 GRCh37 |
1750 | 1805 | |
B4GALT7 | - | - |
GRCh38 GRCh37 |
324 | 414 | |
C5orf60 | - | - | - |
GRCh38 GRCh38 GRCh37 |
- | 42 |
CLK4 | - | - |
GRCh38 GRCh37 |
20 | 59 | |
COL23A1 | - | - |
GRCh38 GRCh37 |
33 | 76 | |
DBN1 | - | - |
GRCh38 GRCh37 |
49 | 112 | |
DOK3 | - | - |
GRCh38 GRCh37 |
46 | 118 | |
F12 | - | - |
GRCh38 GRCh37 |
144 | 225 |
There are 28 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) |
|
Mar 1, 2018 | RCV000846590.2 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Mar 26, 2023