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Variant : CV539455 (GRCh37/hg19 10q26.3(chr10:134609699-135167875)x3) Homo sapiens

Symbol: CV539455
Name: GRCh37/hg19 10q26.3(chr10:134609699-135167875)x3
Condition: See cases [RCV000663392]
Clinical Significance: uncertain significance
Last Evaluated: 10/19/2017
Review Status: criteria provided, single submitter
Related Genes: ADAM8   ADGRA1   CALY   CFAP46   KNDC1   LINC01166   PRAP1   TUBGCP2   UTF1   VENTX   ZNF511  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh3710134,609,699 - 135,167,875CLINVAR
Cytogenetic Map1010q26.3CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13704129
Created: 2018-08-07
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.