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Variant : CV675331 (GRCh37/hg19 7q35(chr7:143572320-144474990)x3) Homo sapiens

Symbol: CV675331
Name: GRCh37/hg19 7q35(chr7:143572320-144474990)x3
Condition: not provided [RCV000848430]
Clinical Significance: uncertain significance
Last Evaluated: 09/17/2018
Review Status: no assertion criteria provided
Related Genes: ARHGEF35   ARHGEF5   CTAGE4   CTAGE8   NOBOX   OR2A1   OR2A12   OR2A14   OR2A2   OR2A25   OR2A42   OR2A5   OR2A7   OR2F1   OR2F2   OR6B1   TCAF1   TPK1  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh377143,572,320 - 144,474,990CLINVAR
Cytogenetic Map77q35CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14979984
Created: 2019-10-08
Species: Homo sapiens
Last Modified: 2020-02-20
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.