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Variant : CV608085 (GRCh37/hg19 Xp22.2(chrX:12927947-13281759)x3) Homo sapiens

Symbol: CV608085
Name: GRCh37/hg19 Xp22.2(chrX:12927947-13281759)x3
Condition: not provided [RCV000753385]
Clinical Significance: benign
Last Evaluated: 04/09/2013
Review Status: no assertion criteria provided
Related Genes: FAM9C   TLR8   TMSB4X  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37X12,927,947 - 13,281,759CLINVAR
Cytogenetic MapXXp22.2CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14350217
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2019-11-05
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.