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Variant : CV383953 (GRCh37/hg19 4q13.2(chr4:67997060-69198391)x3) Homo sapiens

Symbol: CV383953
Name: GRCh37/hg19 4q13.2(chr4:67997060-69198391)x3
Condition: See cases [RCV000447856]
Clinical Significance: uncertain significance
Last Evaluated:
Review Status: no assertion criteria provided
Related Genes: CENPC   GNRHR   STAP1   TMPRSS11A   TMPRSS11B   TMPRSS11D   TMPRSS11F   UBA6   YTHDC1  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37467,997,060 - 69,198,391CLINVAR
Cytogenetic Map44q13.2CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 12852569
Created: 2017-04-11
Species: Homo sapiens
Last Modified: 2020-02-11
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.