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Variant : CV608395 (GRCh37/hg19 Xq22.3(chrX:104768801-104985376)x3) Homo sapiens

Symbol: CV608395
Name: GRCh37/hg19 Xq22.3(chrX:104768801-104985376)x3
Condition: not provided [RCV000753695]
Clinical Significance: benign
Last Evaluated: 01/08/2013
Review Status: no assertion criteria provided
Related Genes: IL1RAPL2  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37X104,768,801 - 104,985,376CLINVAR
Cytogenetic MapXXq22.3CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14350589
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.