GRCh37/hg19 17q23.2-23.3(chr17:58596397-62540700)x3 Detail (hg19) (CD79B, CSH1, CSH2, CSHL1, CYB561, ACE, DDX5, ERN1, GH1, GH2, ICAM2, MAP3K3, PECAM1, PSMC5, SCN4A, SMARCD2, TBX2, PPM1D, TBX4, MRC2, MED13, DCAF7, APPBP2, TLK2, POLG2, DDX42, TANC2, TACO1, BCAS3, TEX2, CCDC47, INTS2, LIMD2, KCNH6, BRIP1, CEP95, STRADA, PRR29, FTSJ3, EFCAB3, MARCHF10, MILR1, METTL2A, NACA2, LINC02875)
Information
Genome
| Assembly | Position |
|---|---|
| hg19 | chr17:58,596,397-62,540,700 |
| hg38 | chr17:60,519,036-64,544,582 |
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
|
criteria provided, single submitter |
unknown
|
Detail |
CIViC
[No Data.]
DisGeNET
[No Data.]
Annotation
Annotations
| Descrption | Source | Links |
|---|---|---|
| GRCh37/hg19 17q23.2-23.3(chr17:58596397-62540700)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
- chr17:58,596,397-62,540,700
- Variant Type
- cnv
Genome browser