ClinVar Genomic variation as it relates to human health
GRCh38/hg38 4q24(chr4:100579010-101522050)x1
Germline
Classification
(1)
Uncertain significance
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 | |||
FLJ20021 | - | - | - | GRCh38 | - | 3 |
LINC01216 | - | - | - | GRCh38 | 1 | 5 |
LINC01217 | - | - | - | GRCh38 | - | 4 |
LINC01218 | - | - | - | GRCh38 | - | 4 |
LOC121725180 | - | - | - | GRCh38 | - | 3 |
LOC123477793 | - | - | - | GRCh38 | - | 8 |
LOC123477794 | - | - | - | GRCh38 | - | 3 |
LOC129992864 | - | - | - | GRCh38 | - | 4 |
LOC129992865 | - | - | - | GRCh38 | - | 4 |
LOC129992866 | - | - | - | GRCh38 | - | 3 |
There are 11 more genes affected by this variant. See the full set of genes in Variation Viewer (GRCh38 , GRCh37 , NCBI36).
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
See cases
|
Uncertain significance (1) |
|
Jan 25, 2013 | RCV000140237.5 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Sep 01, 2024