ClinVar Genomic variation as it relates to human health
GRCh38/hg38 16p13.13(chr16:10778551-11374173)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 | |||
CIITA | - | - |
GRCh38 GRCh37 |
1623 | 1693 | |
CLEC16A | - | - |
GRCh38 GRCh37 |
100 | 129 | |
DEXI | - | - |
GRCh38 GRCh37 |
- | 41 | |
LOC105371083 | - | - | - | GRCh38 | - | 5 |
LOC112296180 | - | - | - | GRCh38 | - | 5 |
LOC116276447 | - | - | - | GRCh38 | - | 6 |
LOC121530617 | - | - | - | GRCh38 | - | 6 |
LOC125146406 | - | - | - | GRCh38 | - | 6 |
LOC125146407 | - | - | - | GRCh38 | - | 6 |
LOC125146408 | - | - | - | GRCh38 | - | 6 |
There are 73 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 | RCV000137607.5 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024