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Variant : CV608336 (GRCh37/hg19 Xq21.2-21.31(chrX:85271998-86201736)x3) Homo sapiens

Symbol: CV608336
Name: GRCh37/hg19 Xq21.2-21.31(chrX:85271998-86201736)x3
Condition: not provided [RCV000753636]
Clinical Significance: benign
Last Evaluated: 06/20/2015
Review Status: no assertion criteria provided
Related Genes: CHM   DACH2  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37X85,271,998 - 86,201,736CLINVAR
Cytogenetic MapXXq21.2-21.31CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14351497
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2019-09-06
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.