ClinVar Genomic variation as it relates to human health
GRCh38/hg38 10q26.3(chr10:131457361-131971639)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 | |||
BNIP3 | - | - |
GRCh38 GRCh37 |
5 | 116 | |
LINC01164 | - | - | - | GRCh38 | - | 45 |
LOC124416935 | - | - | - | GRCh38 | - | 44 |
LOC126861097 | - | - | - | GRCh38 | - | 45 |
LOC126861098 | - | - | - | GRCh38 | - | 44 |
LOC126861099 | - | - | - | GRCh38 | - | 45 |
LOC126861100 | - | - | - | GRCh38 | - | 42 |
LOC130004973 | - | - | - | GRCh38 | - | 45 |
LOC130004974 | - | - | - | GRCh38 | - | 45 |
LOC130004975 | - | - | - | GRCh38 | - | 45 |
There are 6 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 | RCV000051691.4 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Oct 15, 2023