ClinVar Genomic variation as it relates to human health
GRCh37/hg19 16p13.12-13.11(chr16:14643928-14725823)x1
Germline
Classification
(1)
not provided
no classification 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 | |||
BFAR | - | - |
GRCh38 GRCh38 GRCh37 |
19 | 46 | |
NPIPA2 | - | - | - |
GRCh38 GRCh37 |
- | 39 |
NPIPA3 | - | - | - |
GRCh38 GRCh38 GRCh37 |
- | 36 |
PARN | - | - |
GRCh38 GRCh38 GRCh37 |
755 | 782 | |
PLA2G10 | - | - |
GRCh38 GRCh38 GRCh37 |
4 | 39 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
not provided (1) |
|
- | RCV003228701.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 27, 2023