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Variant : CV604565 (GRCh37/hg19 10q26.3(chr10:134889866-135099053)x3) Homo sapiens

Symbol: CV604565
Name: GRCh37/hg19 10q26.3(chr10:134889866-135099053)x3
Condition: not provided [RCV000749865]
Clinical Significance: benign
Last Evaluated: 03/15/2013
Review Status: no assertion criteria provided
Related Genes: ADAM8   ADGRA1   KNDC1   TUBGCP2   UTF1   VENTX  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh3710134,889,866 - 135,099,053CLINVAR
Cytogenetic Map1010q26.3CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14365194
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2020-05-19
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.