GRCh38/hg38 10p12.31(chr10:20776151-21435636)x3 Detail (hg38) (NEBL, NEBL-AS1, LINC02643, LOC111946226, LOC111946227, LOC121366046, LOC124403919, LOC126860875, LOC126860876, LOC130003464, LOC130003465, LOC130003466, LOC132089765)
Information
Genome
| Assembly | Position |
|---|---|
| hg19 | chr10:21,065,080-21,724,565 View the variant detail on this assembly version. |
| hg38 | chr10:20,776,151-21,435,636 |
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
|
2011-08-12 | criteria provided, single submitter |
paternal
|
Detail |
CIViC
[No Data.]
DisGeNET
[No Data.]
Annotation
Annotations
| Descrption | Source | Links |
|---|---|---|
| GRCh38/hg38 10p12.31(chr10:20776151-21435636)x3 AND See cases | ClinVar | Detail |
Overlapped Transcript Coordinates
| Gene | Transcript ID | Exon Number | Chromosome | Start | Stop | Type | Amino Mutation | Transcript Position | Links |
|---|
Overlapped Transcript
| Gene | Transcript ID | Chromosome | Start | Stop | Links |
|---|
- Gene
- -
- Genome
- hg38
- Position
- chr10:20,776,151-21,435,636
- Variant Type
- cnv
Genome browser