GRCh38/hg38 4p15.31(chr4:18360417-19175273)x3 Detail (hg38) (LOC129992316, LOC129992317, LOC129992318)
Information
Genome
| Assembly | Position |
|---|---|
| hg19 | chr4:18,362,040-19,176,896 View the variant detail on this assembly version. |
| hg38 | chr4:18,360,417-19,175,273 |
Summary
MGeND
| Clinical significance | |
| Variant entry | |
| GWAS entry | |
| Disease area statistics | Show details |
ClinVar
| Clinical Significance |
Uncertain significance
|
| Review star |  |
| Show details | |
Links
| Type | Database | ID | Link |
|---|---|---|---|
| Gene | MIM | ||
| HGNC | |||
| Ensembl | |||
| NCBI | |||
| Gene Cards | |||
| OncoKB |
| Type | Database | ID | Link |
|---|---|---|---|
| Variant | TogoVar | ||
| COSMIC | |||
| MONDO |
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
| Clinical significance | Last evaluated | Review status | Condition | Origin | Links |
|---|---|---|---|---|---|
|
Uncertain significance
|
2010-12-22 | no assertion criteria provided |
paternal
|
Detail |
CIViC
[No Data.]
DisGeNET
[No Data.]
Annotation
Genome browser