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Variant : CV555044 (GRCh37/hg19 11q25(chr11:133313372-134110127)x3) Homo sapiens

Symbol: CV555044
Name: GRCh37/hg19 11q25(chr11:133313372-134110127)x3
Condition: not provided [RCV000683349]
Clinical Significance: uncertain significance
Last Evaluated: 11/17/2017
Review Status: no assertion criteria provided
Related Genes: IGSF9B   JAM3   LINC02743   NCAPD3   OPCML   SPATA19   VPS26B  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh3711133,313,372 - 134,110,127CLINVAR
Cytogenetic Map1111q25CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 13796487
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.