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Variant : CV608683 (GRCh37/hg19 Yp11.2(chrY:6214046-6336574)x3) Homo sapiens

Symbol: CV608683
Name: GRCh37/hg19 Yp11.2(chrY:6214046-6336574)x3
Condition: not provided [RCV000753983]
Clinical Significance: benign
Last Evaluated: 09/20/2010
Review Status: no assertion criteria provided
Related Genes: TTTY1B   TTTY21B   TTTY2B   TTTY7  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37Y6,214,046 - 6,336,574CLINVAR
Cytogenetic MapYYp11.2CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14350890
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2020-05-26
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.