ClinVar Genomic variation as it relates to human health
GRCh38/hg38 13q12.12(chr13:22980365-24370481)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 | |||
C1QTNF9 | - | - |
GRCh38 GRCh37 |
27 | 102 | |
C1QTNF9B | - | - |
GRCh38 GRCh37 |
14 | 111 | |
LINC00327 | - | - | - | GRCh38 | - | 36 |
LINC00362 | - | - | - | GRCh38 | - | 43 |
LINC00566 | - | - | - | GRCh38 | - | 28 |
LOC106783494 | - | - | - | GRCh38 | - | 36 |
LOC112163649 | - | - | - | GRCh38 | - | 31 |
LOC121466729 | - | - | - | GRCh38 | - | 31 |
LOC124849295 | - | - | - | GRCh38 | - | 31 |
LOC130009362 | - | - | - | GRCh38 | - | 43 |
There are 47 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) |
|
Mar 9, 2012 | RCV000138208.5 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024