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Variant : CV608091 (GRCh37/hg19 Xp22.2(chrX:15290053-16071445)x3) Homo sapiens

Symbol: CV608091
Name: GRCh37/hg19 Xp22.2(chrX:15290053-16071445)x3
Condition: not provided [RCV000753391]
Clinical Significance: likely benign
Last Evaluated: 12/27/2013
Review Status: no assertion criteria provided
Related Genes: ACE2   AP1S2   ASB11   BMX   CA5B   CLTRN   INE2   PIGA   PIR   VEGFD   ZRSR2  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37X15,290,053 - 16,071,445CLINVAR
Cytogenetic MapXXp22.2CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14350228
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2019-10-08
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.