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Variant : CV437134 (GRCh37/hg19 Xq28(chrX:152559822-153104847)x3) Homo sapiens

Symbol: CV437134
Name: GRCh37/hg19 Xq28(chrX:152559822-153104847)x3
Condition: See cases [RCV000511269]
Clinical Significance: uncertain significance
Last Evaluated: 06/16/2014
Review Status: no assertion criteria provided
Related Genes: ABCD1   ATP2B3   BCAP31   BGN   CCNQ   DUSP9   HAUS7   IDH3G   PDZD4   PLXNB3   PNCK   PNMA6E   SLC6A8   SRPK3   SSR4   TREX2   ZFP92   ZNF275  
Variant Type: copy number gain (SO:0001742)
Evidence: clinical testing
Human AssemblyChrPosition (strand)Source
GRCh37X152,559,822 - 153,104,847CLINVAR
Cytogenetic MapXXq28CLINVAR

References - uncurated

Additional Information

External Database Links
RGD Object Information
RGD ID: 13444244
Created: 2017-11-07
Species: Homo sapiens
Last Modified: 2020-03-24
Status: ACTIVE


RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.