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Variant : CV608545 (GRCh37/hg19 Xq27.3(chrX:142353186-143751508)x3) Homo sapiens

Symbol: CV608545
Name: GRCh37/hg19 Xq27.3(chrX:142353186-143751508)x3
Condition: not provided [RCV000753845]
Clinical Significance: benign
Last Evaluated: 03/23/2013
Review Status: no assertion criteria provided
Related Genes: SLITRK4   SPANXN2   SPANXN3   UBE2NL  
Variant Type: copy number gain (SO:0001742)
Evidence: clinical testing
Human AssemblyChrPosition (strand)Source
GRCh37X142,353,186 - 143,751,508CLINVAR
Cytogenetic MapXXq27.3CLINVAR

Additional Information

External Database Links
CRRD Object Information
CRRD ID: 14350747
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2019-09-10
Status: ACTIVE


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