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Variant : CV608474 (GRCh37/hg19 Xq26.1(chrX:128723451-129281476)x2) Homo sapiens

Symbol: CV608474
Name: GRCh37/hg19 Xq26.1(chrX:128723451-129281476)x2
Condition: not provided [RCV000753774]
Clinical Significance: benign
Last Evaluated: 12/16/2015
Review Status: no assertion criteria provided
Related Genes: AIFM1   APLN   BCORL1   ELF4   OCRL   SASH3   UTP14A   XPNPEP2   ZDHHC9  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37X128,723,451 - 129,281,476CLINVAR
Cytogenetic MapXXq26.1CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14350670
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2019-11-05
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.