ClinVar Genomic variation as it relates to human health
GRCh38/hg38 16q24.2(chr16:87038922-87766879)x1
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 | |||
C16orf95 | - | - | - |
GRCh38 GRCh37 |
1 | 63 |
C16orf95-DT | - | - | - | GRCh38 | - | 27 |
FBXO31 | - | - |
GRCh38 GRCh37 |
67 | 131 | |
JPH3 | - | - |
GRCh38 GRCh37 |
144 | 215 | |
KLHDC4 | - | - |
GRCh38 GRCh37 |
69 | 141 | |
LINC02181 | - | - | - | GRCh38 | - | 22 |
LOC100129215 | - | - | - | GRCh38 | - | 27 |
LOC101928682 | - | - | - | GRCh38 | - | 26 |
LOC101928708 | - | - | - | GRCh38 | - | 26 |
LOC102724467 | - | - | - | GRCh38 | - | 28 |
There are 31 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) |
|
Jul 11, 2011 | RCV000139802.5 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024