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Variant : CV556043 (GRCh37/hg19 Xq13.3-21.1(chrX:75378449-76220379)x2) Homo sapiens

Symbol: CV556043
Name: GRCh37/hg19 Xq13.3-21.1(chrX:75378449-76220379)x2
Condition: not provided [RCV000684348]
Clinical Significance: uncertain significance
Last Evaluated: 02/27/2018
Review Status: no assertion criteria provided
Related Genes: MAGEE1   PBDC1  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37X75,378,449 - 76,220,379CLINVAR
Cytogenetic MapXXq13.3-21.1CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13798636
Created: 2018-10-09
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.