GRCh38/hg38 2p22.3(chr2:32289459-33024069)x3 Detail (hg38) (LTBP1, TTC27, BIRC6, YIPF4, LINC00486, MIR558, LOC100271832, MIR4765, BIRC6-AS2, LOC112840924, LOC112840925, LOC122756687, LOC126806184, LOC129933458, LOC129933459, LOC129933460, LOC129933461, LOC129933462, LOC132088840)
Information
Genome
| Assembly | Position |
|---|---|
| hg19 | chr2:32,514,528-33,249,136 View the variant detail on this assembly version. |
| hg38 | chr2:32,289,459-33,024,069 |
Summary
MGeND
| Clinical significance | |
| Variant entry | |
| GWAS entry | |
| Disease area statistics | Show details |
ClinVar
| Clinical Significance |
Benign
|
| 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 |
|---|---|---|---|---|---|
|
Benign
|
2010-10-14 | no assertion criteria provided |
not provided
|
Detail |
CIViC
[No Data.]
DisGeNET
[No Data.]
Annotation
Annotations
| Descrption | Source | Links |
|---|---|---|
| GRCh38/hg38 2p22.3(chr2:32289459-33024069)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
- chr2:32,289,459-33,024,069
- Variant Type
- cnv
Genome browser