ClinVar Genomic variation as it relates to human health
GRCh38/hg38 16q24.1(chr16:85026633-85843419)x3
Germline
Classification
(1)
Likely benign
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 | |||
C16orf74 | - | - | - |
GRCh38 GRCh37 |
4 | 60 |
CIBAR2 | - | - |
GRCh38 GRCh37 |
41 | 97 | |
COX4I1 | - | - |
GRCh38 GRCh37 |
21 | 76 | |
EMC8 | - | - |
GRCh38 GRCh37 |
9 | 63 | |
GINS2 | - | - |
GRCh38 GRCh37 |
24 | 79 | |
GSE1 | - | - |
GRCh38 GRCh37 |
194 | 252 | |
KIAA0513 | - | - |
GRCh38 GRCh37 |
30 | 89 | |
LINC00311 | - | - | - | GRCh38 | - | 22 |
LINC02139 | - | - | - | GRCh38 | - | 22 |
LOC101928557 | - | - | - | GRCh38 | - | 22 |
There are 64 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
|
Likely benign (1) |
|
Oct 10, 2011 | RCV000138715.5 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024