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Variant : CV613952 (GRCh37/hg19 Yp11.32-q11.221(chrY:1640371-19565713)) Homo sapiens

Symbol: CV613952
Name: GRCh37/hg19 Yp11.32-q11.221(chrY:1640371-19565713)
Condition: not provided [RCV000767656]
Clinical Significance: pathogenic
Last Evaluated: 11/01/2018
Review Status: criteria provided, single submitter
Related Genes: AMELY   DDX3Y   FAM197Y1   FAM197Y9   NLGN4Y   PCDH11Y   RPS4Y1   SRY   TBL1Y   TGIF2LY   TMSB4Y   TSPY1   TSPY10   TSPY2   TSPY3   TSPY4   TSPY8   TTTY1   TTTY11   TTTY12   TTTY13B   TTTY15   TTTY16   TTTY18   TTTY19   TTTY1B   TTTY2   TTTY20   TTTY21   TTTY21B   TTTY22   TTTY23   TTTY23B   TTTY2B   TTTY7   TTTY7B   TTTY8   TTTY8B   USP9Y   UTY   VCY   VCY1B   ZFY  
Variant Type: copy number gain (SO:0001742)
Evidence: clinical testing
Human AssemblyChrPosition (strand)Source
GRCh37Y1,640,371 - 19,565,713CLINVAR
Cytogenetic MapYYp11.32-q11.221CLINVAR

References - uncurated

Additional Information

External Database Links
CRRD Object Information
CRRD ID: 14399619
Created: 2019-05-07
Species: Homo sapiens
Last Modified: 2020-05-12
Status: ACTIVE


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