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Variant : CV608701 (GRCh37/hg19 Yp11.2(chrY:9524637-9968357)x0) Homo sapiens

Symbol: CV608701
Name: GRCh37/hg19 Yp11.2(chrY:9524637-9968357)x0
Condition: not provided [RCV000754001]
Clinical Significance: benign
Last Evaluated: 10/05/2012
Review Status: no assertion criteria provided
Related Genes: TTTY1   TTTY2   TTTY21   TTTY22   TTTY23   TTTY7B   TTTY8  
Variant Type: copy number loss (SO:0001743)
Evidence: clinical testing
Human AssemblyChrPosition (strand)Source
GRCh37Y9,524,637 - 9,968,357CLINVAR
Cytogenetic MapYYp11.2CLINVAR

Additional Information

External Database Links
CRRD Object Information
CRRD ID: 14350908
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2020-05-26
Status: ACTIVE


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