ClinVar Genomic variation as it relates to human health
NC_000023.10:g.(?_99551275)_(101097764_?)del
Germline
Classification
(1)
Pathogenic
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 | |||
BTK | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
708 | 885 | |
GLA | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
6 | 1244 | |
PCDH19 | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
1180 | 1485 | |
TIMM8A | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
59 | 234 | |
NXF5 | Little evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
77 | 236 | |
SRPX2 | No evidence available | No evidence available |
GRCh38 GRCh37 |
165 | 340 | |
ARL13A | - | - | - |
GRCh38 GRCh37 |
- | 171 |
ARMCX1 | - | - |
GRCh38 GRCh37 |
16 | 176 | |
ARMCX2 | - | - |
GRCh38 GRCh37 |
27 | 187 | |
ARMCX3 | - | - |
GRCh38 GRCh37 |
8 | 169 |
There are 17 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 |
---|---|---|---|---|
Pathogenic (1) |
|
Aug 15, 2022 | RCV003113386.4 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Jun 10, 2024