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Variant : CV383007 (GRCh37/hg19 Xp22.2(chrX:15445440-16061424)x2) Homo sapiens

Symbol: CV383007
Name: GRCh37/hg19 Xp22.2(chrX:15445440-16061424)x2
Condition: See cases [RCV000445674]
Clinical Significance: uncertain significance
Last Evaluated:
Review Status: no assertion criteria provided
Related Genes: ACE2   AP1S2   BMX   CA5B   CLTRN   INE2   PIR   ZRSR2  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37X15,445,440 - 16,061,424CLINVAR
Cytogenetic MapXXp22.2CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 12850408
Created: 2017-04-11
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.