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Variant : CV486691 (t(6;9)(q23.3;p22.3)) Homo sapiens

Symbol: CV486691
Name: t(6;9)(q23.3;p22.3)
Condition: Adenoid cystic carcinoma [RCV000585766]
Clinical Significance: pathogenic
Last Evaluated: 02/01/2018
Review Status: no assertion criteria provided
Related Genes: MYB   NFIB  
Variant Type: translocation (SO:0000199)
Source: CLINVAR
Evidence: research
Position
Human AssemblyChrPosition (strand)Source
GRCh376135,522,688 - 135,522,689CLINVAR
GRCh37914,093,875 - 14,093,876CLINVAR
Cytogenetic Map66q23.3CLINVAR
Cytogenetic Map99p23CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 13517307
Created: 2018-04-10
Species: Homo sapiens
Last Modified: 2019-11-12
Status: ACTIVE



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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.