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Variant : CV608698 (GRCh37/hg19 Yp11.2(chrY:9507451-9645004)x0) Homo sapiens

Symbol: CV608698
Name: GRCh37/hg19 Yp11.2(chrY:9507451-9645004)x0
Condition: not provided [RCV000753998]
Clinical Significance: benign
Last Evaluated: 10/15/2010
Review Status: no assertion criteria provided
Related Genes: TTTY1   TTTY2   TTTY21   TTTY22   TTTY7B   TTTY8  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37Y9,507,451 - 9,645,004CLINVAR
Cytogenetic MapYYp11.2CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14350905
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2020-05-19
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.