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Variant : CV436992 (GRCh37/hg19 Xp22.13(chrX:17674125-17991059)x2) Homo sapiens

Symbol: CV436992
Name: GRCh37/hg19 Xp22.13(chrX:17674125-17991059)x2
Condition: See cases [RCV000512183]
Clinical Significance: uncertain significance
Last Evaluated: 09/09/2015
Review Status: no assertion criteria provided
Related Genes: NHS   RAI2   SCML1  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37X17,674,125 - 17,991,059CLINVAR
Cytogenetic MapXXp22.13CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13445150
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.