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Variant : CV436741 (GRCh37/hg19 Xp22.2-22.13(chrX:16985921-17731101)x2) Homo sapiens

Symbol: CV436741
Name: GRCh37/hg19 Xp22.2-22.13(chrX:16985921-17731101)x2
Condition: See cases [RCV000510220]
Clinical Significance: uncertain significance
Last Evaluated: 12/02/2014
Review Status: no assertion criteria provided
Related Genes: NHS   REPS2  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37X16,985,921 - 17,731,101CLINVAR
Cytogenetic MapXXp22.2-22.13CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13443200
Created: 2017-11-07
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.