ClinVar Genomic variation as it relates to human health
NC_000015.9:g.(?_89379429)_(91565479_?)dup
Germline
Classification
(2)
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 | |||
ABHD2 | - | - |
GRCh38 GRCh37 |
15 | 56 | |
ACAN | - | - |
GRCh38 GRCh37 |
1059 | 1095 | |
ANPEP | - | - |
GRCh38 GRCh37 |
48 | 104 | |
AP3S2 | - | - |
GRCh38 GRCh37 |
- | 52 | |
ARPIN | - | - |
GRCh38 GRCh37 |
- | 61 | |
ARPIN-AP3S2 | - | - | - |
GRCh38 GRCh37 |
- | 65 |
BLM | - | - |
GRCh38 GRCh37 |
4169 | 4224 | |
CIB1 | - | - |
GRCh38 GRCh37 |
137 | 225 | |
CRTC3 | - | - |
GRCh38 GRCh37 |
6 | 68 | |
FANCI | - | - |
GRCh38 GRCh37 |
1947 | 2143 |
There are 29 more genes affected by this variant. See the full set of genes in Variation Viewer (GRCh37).
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Sep 1, 2022 | RCV003111027.3 | |
no classifications from unflagged records (1) |
|
- | RCV003111026.5 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Dec 09, 2023