ClinVar Genomic variation as it relates to human health
GRCh37/hg19 5p13.2-11(chr5:36053583-46389339)x3
Germline
Classification
(1)
Pathogenic
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 | |||
NIPBL | Sufficient evidence for dosage pathogenicity | Little evidence for dosage pathogenicity |
GRCh38 GRCh37 |
1797 | 1851 | |
FGF10 | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
80 | 110 | |
ANXA2R | - | - |
GRCh38 GRCh37 |
- | 41 | |
C5orf34 | - | - | - |
GRCh38 GRCh37 |
2 | 31 |
C6 | - | - |
GRCh38 GRCh37 |
472 | 494 | |
C7 | - | - |
GRCh38 GRCh37 |
536 | 559 | |
C9 | - | - |
GRCh38 GRCh37 |
322 | 347 | |
CARD6 | - | - |
GRCh38 GRCh37 |
70 | 91 | |
CCDC152 | - | - | - |
GRCh38 GRCh37 |
16 | 57 |
CCL28 | - | - |
GRCh38 GRCh37 |
7 | 31 |
There are 37 more genes affected by this variant. See the full set of genes in Variation Viewer (GRCh37) and ClinGen Dosage Sensitivity Map.
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
musculoskeletal system issues
|
Pathogenic (1) |
|
- | RCV002284293.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Sep 24, 2022