ClinVar Genomic variation as it relates to human health
GRCh38/hg38 10p15.1(chr10:5406594-5566679)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 | |||
CALML3 | - | - |
GRCh38 GRCh37 |
- | 44 | |
CALML3-AS1 | - | - | - |
GRCh38 GRCh37 |
- | 44 |
CALML5 | - | - |
GRCh38 GRCh37 |
7 | 42 | |
LOC116216110 | - | - | - | GRCh38 | - | 18 |
LOC116216111 | - | - | - | GRCh38 | - | 18 |
LOC121811724 | - | - | - | GRCh38 | - | 18 |
LOC130003193 | - | - | - | GRCh38 | - | 18 |
LOC130003194 | - | - | - | GRCh38 | - | 18 |
LOC132089787 | - | - | - | GRCh38 | - | 18 |
LOC132089788 | - | - | - | GRCh38 | - | 18 |
There is 1 more gene 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) |
|
Nov 30, 2010 | RCV000141298.3 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Oct 15, 2023