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Variant : CV435954 (GRCh37/hg19 Xq23-24(chrX:111149921-117993284)x3) Homo sapiens

Symbol: CV435954
Name: GRCh37/hg19 Xq23-24(chrX:111149921-117993284)x3
Condition: See cases [RCV000510739]
Clinical Significance: likely pathogenic
Last Evaluated: 02/01/2016
Review Status: no assertion criteria provided
Related Genes: AGTR2   AMOT   CT83   DANT2   DOCK11   HTR2C   IL13RA1   IL13RA2   KLHL13   LHFPL1   LRCH2   LUZP4   MIR448   PLS3   RBMXL3   RTL4   SLC6A14   TRPC5   WDR44   ZCCHC12  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37X111,149,921 - 117,993,284CLINVAR
Cytogenetic MapXXq23-24CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13443717
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.