Genomic Map
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Target Gene Details
Entrez Gene ID: | 10673 |
Gene Name: | tumor necrosis factor superfamily member 13b |
Gene Aliases: |
BAFF, BLYS, CD257, DTL, TALL-1, TALL1, THANK, TNFSF20, TNLG7A, ZTNF4 |
Location: |
Chr.13:108268240-108308484 on Build GRCh38 |
Assay Gene Location: | Overlaps Exon 2 - Intron 2 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| TNFSF13B | NM_001145645.2 | NP_001139117.1 | ||
| NM_006573.4 | NP_006564.1 | |||
| AF116456.1 | AAD25356.1 | |||
| AF132600.1 | AAD21092.1 | |||
| AF134715.1 | AAF60219.1 | |||
| AF136293.1 | AAD29421.1 | |||
| AF186114.1 | AAF01432.1 | |||
| AK309629.1 | ||||
| AY129225.1 | AAN08421.1 | |||
| AY129226.1 | AAN08422.1 | |||
| AY129227.1 | AAN08423.1 | |||
| AY129228.1 | AAN08424.1 | |||
| AY302751.1 | AAP83164.1 | |||
| AY358881.1 | AAQ89240.1 | |||
| BC020674.1 | AAH20674.1 | |||
| BI818459.1 | ||||
| CR541818.1 | CAG46617.1 | |||
| HM636064.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv951917 | Chr.13:108263353 - 108270752 on Build GRCh38 | Duplication |
 TNFSF13B
|
| esv2747975 | Chr.13:108256752 - 108796958 on Build GRCh38 | Deletion |
MYO16
TNFSF13B
|
| nsv1139838 | Chr.13:108256721 - 108796820 on Build GRCh38 | Deletion |
MYO16
TNFSF13B
|
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Set Membership: |
Intragenic
Non-exonic
DGV Variation
|
Gene Ontology Categories:
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