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Variant : CV554929 (GRCh37/hg19 10q26.13(chr10:126319221-126733607)x3) Homo sapiens

Symbol: CV554929
Name: GRCh37/hg19 10q26.13(chr10:126319221-126733607)x3
Condition: not provided [RCV000683234]
Clinical Significance: uncertain significance
Last Evaluated: 04/13/2018
Review Status: no assertion criteria provided
Related Genes: ABRAXAS2   CTBP2   EEF1AKMT2   FAM53B   ZRANB1  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh3710126,319,221 - 126,733,607CLINVAR
Cytogenetic Map1010q26.13CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13796269
Created: 2018-10-09
Species: Homo sapiens
Last Modified: 2020-07-28
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.