ClinVar Genomic variation as it relates to human health
GRCh38/hg38 9q21.31-21.32(chr9:78805124-81880860)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 | |||
LINC01507 | - | - | - | GRCh38 | - | 16 |
LNCARSR | - | - | - | GRCh38 | - | 16 |
LOC101927450 | - | - | - | GRCh38 | - | 16 |
LOC110120622 | - | - | - | GRCh38 | - | 14 |
LOC110120660 | - | - | - | GRCh38 | - | 16 |
LOC110120661 | - | - | - | GRCh38 | - | 16 |
LOC110120702 | - | - | - | GRCh38 | - | 14 |
LOC110120754 | - | - | - | GRCh38 | - | 14 |
LOC110120764 | - | - | - | GRCh38 | - | 16 |
LOC110120816 | - | - | - | GRCh38 | - | 14 |
There are 30 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) |
|
Aug 12, 2011 | RCV000052231.5 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Oct 15, 2023