ClinVar Genomic variation as it relates to human health
GRCh38/hg38 19q13.11(chr19:32469643-32843761)x1
Germline
Classification
(1)
Uncertain significance
criteria provided, single submitter
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 | |||
ANKRD27 | - | - |
GRCh38 GRCh37 |
75 | 91 | |
DPY19L3 | - | - |
GRCh38 GRCh37 |
40 | 58 | |
LOC121627869 | - | - | - | GRCh38 | - | 7 |
LOC121627870 | - | - | - | GRCh38 | - | 7 |
LOC121852986 | - | - | - | GRCh38 | - | 7 |
LOC126862892 | - | - | - | GRCh38 | - | 7 |
LOC126862893 | - | - | - | GRCh38 | - | 7 |
LOC130064158 | - | - | - | GRCh38 | - | 7 |
LOC130064159 | - | - | - | GRCh38 | - | 7 |
LOC130064160 | - | - | - | GRCh38 | - | 8 |
There are 11 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) |
|
Aug 12, 2011 | RCV000052094.5 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Oct 15, 2023