ClinVar Genomic variation as it relates to human health
NC_000016.9:g.(?_2029297)_(2096295_?)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 | |||
GFER | - | - |
GRCh38 GRCh38 GRCh37 |
91 | 208 | |
NHERF2 | - | - |
GRCh38 GRCh37 |
51 | 106 | |
NOXO1 | - | - |
GRCh38 GRCh38 GRCh37 |
- | 105 | |
NPW | - | - |
GRCh38 GRCh38 GRCh37 |
8 | 70 | |
NTHL1 | - | - |
GRCh38 GRCh37 |
1520 | 1641 | |
SYNGR3 | - | - |
GRCh38 GRCh38 GRCh37 |
17 | 79 | |
ZNF598 | - | - |
GRCh38 GRCh38 GRCh37 |
38 | 96 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Pathogenic (1) |
|
Dec 26, 2022 | RCV001958665.4 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Jun 17, 2024