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Variant : CV556152 (GRCh37/hg19 Yp11.32-q11.1(chrY:168807-13134517)x1,2) Homo sapiens

Symbol: CV556152
Name: GRCh37/hg19 Yp11.32-q11.1(chrY:168807-13134517)x1,2
Condition: not provided [RCV000684443]
Clinical Significance: pathogenic
Last Evaluated: 12/30/2017
Review Status: no assertion criteria provided
Related Genes: AMELY   FAM197Y1   FAM197Y9   PCDH11Y   RPS4Y1   SRY   TBL1Y   TGIF2LY   TSPY1   TSPY10   TSPY2   TSPY3   TSPY4   TSPY8   TTTY1   TTTY11   TTTY12   TTTY13B   TTTY16   TTTY18   TTTY19   TTTY1B   TTTY2   TTTY20   TTTY21   TTTY21B   TTTY22   TTTY23   TTTY23B   TTTY2B   TTTY7   TTTY7B   TTTY8   TTTY8B   ZFY  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37Y168,807 - 13,134,517CLINVAR
Cytogenetic MapYYp11.32-q11.1CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13798679
Created: 2018-10-09
Species: Homo sapiens
Last Modified: 2020-05-12
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.