ClinVar Genomic variation as it relates to human health
GRCh38/hg38 17q25.3(chr17:81885863-82358856)x3
Germline
Classification
(1)
Uncertain significance
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 | |||
ALYREF | - | - |
GRCh38 GRCh37 |
- | 27 | |
ANAPC11 | - | - |
GRCh38 GRCh37 |
4 | 31 | |
ASPSCR1 | - | - |
GRCh38 GRCh37 |
45 | 71 | |
CCDC57 | - | - | - |
GRCh38 GRCh37 |
62 | 90 |
CD7 | - | - |
GRCh38 GRCh37 |
17 | 44 | |
CENPX | - | - |
GRCh38 GRCh37 |
1 | 27 | |
CSNK1D | - | - |
GRCh38 GRCh37 |
13 | 41 | |
DCXR | - | - |
GRCh38 GRCh37 |
14 | 52 | |
DCXR-DT | - | - | - | GRCh38 | - | 9 |
DUS1L | - | - | - |
GRCh38 GRCh37 |
35 | 61 |
There are 87 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 |
---|---|---|---|---|
Uncertain significance (1) |
|
Aug 12, 2011 | RCV000054049.5 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Oct 15, 2023