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Variant : CV163725 (GRCh38/hg38 Xq28(chrX:153392250-153934599)x3) Homo sapiens

Symbol: CV163725
Name: GRCh38/hg38 Xq28(chrX:153392250-153934599)x3
Condition: See cases [RCV000142157]
Clinical Significance: uncertain significance
Last Evaluated: 10/29/2013
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: ABCD1   ARHGAP4   ATP2B3   AVPR2   BCAP31   BGN   CCNQ   DUSP9   HAUS7   IDH3G   L1CAM   NAA10   PDZD4   PLXNB3   PNCK   PNMA6E   SLC6A8   SRPK3   SSR4   TREX2   ZFP92  
Variant Type: copy number gain (SO:0001742)
Evidence: clinical testing
HGVS Name(s): NC_000023.11:g.(?_153392250)_(153934599_?)dup
Human AssemblyChrPosition (strand)Source
GRCh38X153,392,250 - 153,934,599CLINVAR
GRCh37X152,657,708 - 153,200,052CLINVAR
Build 36X152,310,902 - 152,853,246CLINVAR
Cytogenetic MapXXq28CLINVAR

References - uncurated

Additional Information

External Database Links
RGD Object Information
RGD ID: 9489676
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-03-31
Status: ACTIVE


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