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Variant : CV608623 (GRCh37/hg19 Xq28(chrX:152932626-153008731)x2) Homo sapiens

Symbol: CV608623
Name: GRCh37/hg19 Xq28(chrX:152932626-153008731)x2
Condition: not provided [RCV000753923]
Clinical Significance: benign
Last Evaluated: 03/11/2013
Review Status: no assertion criteria provided
Related Genes: ABCD1   BCAP31   PNCK   SLC6A8  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37X152,932,626 - 153,008,731CLINVAR
Cytogenetic MapXXq28CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14350828
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2019-09-10
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.