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Variant : CV675490 (GRCh37/hg19 Xq28(chrX:152405258-152942804)x3) Homo sapiens

Symbol: CV675490
Name: GRCh37/hg19 Xq28(chrX:152405258-152942804)x3
Condition: not provided [RCV000848589]
Clinical Significance: uncertain significance
Last Evaluated: 06/28/2018
Review Status: no assertion criteria provided
Related Genes: ATP2B3   BGN   CCNQ   DUSP9   HAUS7   MAGEA1   PNCK   PNMA6E   TREX2   ZFP92   ZNF275  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37X152,405,258 - 152,942,804CLINVAR
Cytogenetic MapXXq28CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 14980134
Created: 2019-10-08
Species: Homo sapiens
Last Modified: 2020-03-24
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.