GRCh38/hg38 7p14.3(chr7:29030620-29796236)x1 Detail (hg19) (CHN2, CPVL, PRR15, LOC646762, MIR550A3, CHN2-AS1, PRR15-DT, LOC116183088, LOC123956125, LOC123956126, LOC126859978, LOC126859979, LOC129389776, LOC129998163, LOC129998164)
Information
Genome
| Assembly | Position |
|---|---|
| hg19 | chr7:29,070,236-29,835,852 |
| hg38 | chr7:29,030,620-29,796,236 View the variant detail on this assembly version. |
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
|
2012-10-15 | no assertion criteria provided |
not provided
|
Detail |
CIViC
[No Data.]
DisGeNET
[No Data.]
Annotation
Annotations
| Descrption | Source | Links |
|---|---|---|
| GRCh38/hg38 7p14.3(chr7:29030620-29796236)x1 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
- hg19
- Position
- chr7:29,070,236-29,835,852
- Variant Type
- cnv
Genome browser