ClinVar Genomic variation as it relates to human health
NC_000001.11:g.112796384_112887499dup
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 | |||
MOV10 | No evidence available | No evidence available |
GRCh38 GRCh37 |
55 | 77 | |
CAPZA1 | - | - |
GRCh38 GRCh37 |
20 | 42 | |
LINC01356 | - | - | - | GRCh38 | - | 6 |
LINC01357 | - | - | - | GRCh38 | - | 6 |
LOC122094900 | - | - | - | GRCh38 | - | 6 |
LOC129388586 | - | - | - | GRCh38 | - | 6 |
LOC129931216 | - | - | - | GRCh38 | - | 6 |
LOC129931217 | - | - | - | GRCh38 | - | 6 |
LRIG2 | - | - |
GRCh38 GRCh37 |
108 | 133 | |
MIR11399 | - | - | - | GRCh38 | - | 6 |
There are 4 more genes affected by this variant. See the full set of genes in Variation Viewer (GRCh38 , GRCh37) and ClinGen Dosage Sensitivity Map.
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Jun 1, 2018 | RCV000754395.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Oct 15, 2023