ClinVar Genomic variation as it relates to human health
GRCh38/hg38 19p13.11-12(chr19:19859042-20621825)x3
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 | |||
ERVS71-1 | - | - | - | GRCh38 | 1 | 8 |
LOC125371497 | - | - | - | GRCh38 | - | 6 |
LOC126862884 | - | - | - | GRCh38 | - | 6 |
LOC130064091 | - | - | - | GRCh38 | - | 6 |
LOC130064092 | - | - | - | GRCh38 | - | 6 |
LOC130064093 | - | - | - | GRCh38 | - | 7 |
LOC130064094 | - | - | - | GRCh38 | - | 7 |
LOC130064095 | - | - | - | GRCh38 | - | 7 |
MIR1270 | - | - | - | GRCh38 | - | 7 |
ZNF253 | - | - |
GRCh38 GRCh37 |
28 | 42 |
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) |
|
Nov 4, 2011 | RCV000137936.5 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024