ClinVar Genomic variation as it relates to human health
GRCh37/hg19 7p15.3(chr7:22574536-23357770)
Germline
Classification
(1)
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 | |||
GPNMB | - | - |
GRCh38 GRCh37 |
74 | 106 | |
HYCC1 | - | - |
GRCh38 GRCh37 |
337 | 376 | |
IGF2BP3 | - | - |
GRCh38 GRCh37 |
25 | 58 | |
IL6 | - | - |
GRCh38 GRCh37 |
6 | 49 | |
IL6-AS1 | - | - | - |
GRCh38 GRCh37 |
- | 43 |
KLHL7 | - | - |
GRCh38 GRCh37 |
351 | 386 | |
KLHL7-DT | - | - | - |
GRCh38 GRCh37 |
- | 35 |
MALSU1 | - | - |
GRCh38 GRCh37 |
10 | 59 | |
NUP42 | - | - |
GRCh38 GRCh37 |
24 | 62 | |
TOMM7 | - | - |
GRCh38 GRCh37 |
6 | 40 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Mar 1, 2022 | RCV002053673.3 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Aug 16, 2022