GRCh38/hg38 19p13.12(chr19:14477761-15133653)x3 Detail (hg19) (DNAJB1, NDUFB7, SLC1A6, TECR, GIPC1, ILVBL, CASP14, OR7A17, OR7C2, OR7A5, OR7C1, ADGRE2, ZNF333, ADGRE3, SYDE1, OR1I1, TEKTL1, CLEC17A, OR7A10, MIR639, SNORA104, LOC113939968, LOC116276506, ILVBL-AS1, LOC126862869, LOC126862870, LOC130063790, LOC130063791, LOC130063792, LOC130063793, LOC130063794, LOC130063795, LOC130063796, LOC130063797, LOC130063798, LOC130063799, LOC130063800, LOC130063801, LOC130063802, LOC130063803, LOC130063804, LOC130063805, LOC130063806)
Information
Genome
| Assembly | Position |
|---|---|
| hg19 | chr19:14,588,573-15,244,464 |
| hg38 | chr19:14,477,761-15,133,653 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
|
2010-02-28 | no assertion criteria provided |
not provided
|
Detail |
CIViC
[No Data.]
DisGeNET
[No Data.]
Annotation
Annotations
| Descrption | Source | Links |
|---|---|---|
| GRCh38/hg38 19p13.12(chr19:14477761-15133653)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
- hg19
- Position
- chr19:14,588,573-15,244,464
- Variant Type
- cnv
Genome browser