GRCh38/hg38 3q13.32-13.33(chr3:117844958-120826621)x4 Detail (hg38) (ADPRH, CD80, GSK3B, GTF2E1, HGD, NDUFB4, UPK1B, B4GALT4, NR1I2, COX17, FSTL1, TIMMDC1, PLA1A, TMEM39A, POGLUT1, ARHGAP31, POPDC2, CFAP91, LRRC58, IGSF11, TEX55, GPR156, RABL3, MIR198, BTNL12P, IGSF11-AS1, B4GALT4-AS1, ARHGAP31-AS1, LOC101926968, LINC02049, LOC105374060, GSK3B-DT, LOC112848344, LOC112872290, LOC112872291, MIR6529, LOC115995517, LOC121725153, LOC123038158, LOC123038159, LOC123038160, LOC126806780, LOC126806781, LOC126806782, LOC126806783, LOC126806784, LOC126806785, LOC126806786, LINC03051, LOC129389114, LOC129389115, LOC129389116, LOC129389117, LOC129937292, LOC129937293, LOC129937294, LOC129937295, LOC129937296, LOC129937297, LOC129937298, LOC129937299, LOC129937300, LOC129937301, LOC129937302, LOC129937303, LOC129937304, LOC129937305, LOC129937306, LOC129937307, LOC129937308, LOC129937309, LOC129937310, LOC129937311, LOC129937312, LOC129937313, LOC129937314, LOC129937315, LOC129937316, LOC129937317, LOC129937318, LOC129937319, LOC129937320, LOC129937321, LOC129937322, LOC129937323, LOC129937324, LOC129937325, LOC129937326, LOC129937327, LOC129937328, LOC129937329, LOC129937330, LOC129937331, LOC129937332, LOC129937333, LOC129937334, LOC129937335, LOC129937336, LOC129937337, LOC129937338, LOC129937339, LOC129937340, LOC129937341)
Information
Genome
| Assembly | Position |
|---|---|
| hg19 | chr3:117,563,805-120,545,468 View the variant detail on this assembly version. |
| hg38 | chr3:117,844,958-120,826,621 |
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
|
2013-09-27 | no assertion criteria provided |
maternal
|
Detail |
CIViC
[No Data.]
DisGeNET
[No Data.]
Annotation
Annotations
| Descrption | Source | Links |
|---|---|---|
| GRCh38/hg38 3q13.32-13.33(chr3:117844958-120826621)x4 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
- chr3:117,844,958-120,826,621
- Variant Type
- cnv
Genome browser