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Variant : CV155753 (GRCh38/hg38 Xq21.1-21.2(chrX:81930916-85965282)x1) Homo sapiens

Symbol: CV155753
Name: GRCh38/hg38 Xq21.1-21.2(chrX:81930916-85965282)x1
Condition: See cases [RCV000135328]
Clinical Significance: pathogenic
Last Evaluated: 11/30/2010
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: APOOL   CHM   CYLC1   HDX   MIR1321   MIR361   MIR548I4   POF1B   POU3F4   RPS6KA6   SATL1   ZNF711  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000023.11:g.(?_81930916)_(85965282_?)del
NC_000023.10:g.(?_81186415)_(85220287_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh38X81,930,916 - 85,965,282CLINVAR
GRCh37X81,186,415 - 85,220,287CLINVAR
Build 36X81,073,071 - 85,106,943CLINVAR
Cytogenetic MapXXq21.1-21.2CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9482901
Created: 2014-09-09
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.