ClinVar Genomic variation as it relates to human health
GRCh38/hg38 8p23.1(chr8:10379998-10970694)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 | |||
C8orf74 | - | - | - |
GRCh38 GRCh38 GRCh37 |
5 | 131 |
CRE3 | - | - | - |
GRCh38 GRCh38 |
- | 57 |
LINC03022 | - | - | - |
GRCh38 GRCh38 |
- | 59 |
LOC102723313 | - | - | - |
GRCh38 GRCh38 |
- | 92 |
LOC129389955 | - | - | - |
GRCh38 GRCh38 |
- | 57 |
LOC129999850 | - | - | - |
GRCh38 GRCh38 |
- | 59 |
LOC129999851 | - | - | - |
GRCh38 GRCh38 |
- | 57 |
LOC129999852 | - | - | - |
GRCh38 GRCh38 |
- | 57 |
LOC129999853 | - | - | - |
GRCh38 GRCh38 |
- | 57 |
LOC129999854 | - | - | - |
GRCh38 GRCh38 |
- | 56 |
There are 10 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
|
Uncertain significance (1) |
|
Sep 21, 2012 | RCV000139604.5 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024