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Variant : CV556014 (GRCh37/hg19 Xp11.4(chrX:37785553-38011836)x2) Homo sapiens

Symbol: CV556014
Name: GRCh37/hg19 Xp11.4(chrX:37785553-38011836)x2
Condition: not provided [RCV000684319]
Clinical Significance: uncertain significance
Last Evaluated: 10/13/2017
Review Status: no assertion criteria provided
Related Genes: H2AP   SRPX   SYTL5  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37X37,785,553 - 38,011,836CLINVAR
Cytogenetic MapXXp11.4CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13798652
Created: 2018-10-09
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.