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Variant : CV248205 (GRCh37/hg19 Xq13.1(chrX:70459474-70654410)x2) Homo sapiens

Symbol: CV248205
Name: GRCh37/hg19 Xq13.1(chrX:70459474-70654410)x2
Condition: See cases [RCV000240450]
Clinical Significance: uncertain significance
Last Evaluated: 01/20/2016
Review Status: criteria provided, single submitter
Related Genes: ITGB1BP2   NONO   TAF1   ZMYM3  
Variant Type: copy number gain (SO:0001742)
Evidence: clinical testing
Human AssemblyChrPosition (strand)Source
GRCh37X70,459,474 - 70,654,410CLINVAR
Cytogenetic MapXXq13.1CLINVAR

Additional Information

External Database Links
CRRD Object Information
CRRD ID: 11541845
Created: 2016-10-11
Species: Homo sapiens
Last Modified: 2019-10-08
Status: ACTIVE


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