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Variant : CV603075 (GRCh37/hg19 9p21.1-13.3(chr9:32912345-33564154)x3) Homo sapiens

Symbol: CV603075
Name: GRCh37/hg19 9p21.1-13.3(chr9:32912345-33564154)x3
Condition: not provided [RCV000748375]
Clinical Significance: benign
Last Evaluated: 10/20/2011
Review Status: no assertion criteria provided
Related Genes: ANKRD18B   APTX   AQP3   AQP7   B4GALT1   BAG1   CHMP5   DNAJA1   NFX1   NOL6   SMU1   SPINK4  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37932,912,345 - 33,564,154CLINVAR
Cytogenetic Map99p21.1-13.3CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14363708
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2019-12-03
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.