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Variant : CV71865 (GRCh38/hg38 Yp11.2-q11.223(chrY:2786811-22358529)x2) Homo sapiens

Symbol: CV71865
Name: GRCh38/hg38 Yp11.2-q11.223(chrY:2786811-22358529)x2
Condition: See cases [RCV000050942]
Clinical Significance: pathogenic
Last Evaluated: 08/12/2011
Review Status: classified by single submitter|criteria provided, single submitter|no assertion criteria provided
Related Genes: AMELY   CDY2A   CDY2B   DDX3Y   EIF1AY   FAM197Y1   FAM197Y2   FAM197Y3   FAM197Y4   FAM197Y5   FAM197Y6   FAM197Y7   FAM197Y8   FAM197Y9   FAM224A   FAM224B   FAM41AY1   FAM41AY2   HSFY1   HSFY2   KDM5D   LINC00278   LINC00279   LINC00280   MIR12120   MIR9985   NLGN4Y   NLGN4Y-AS1   PCDH11Y   PRORY   PRY2   RBMY1A1   RBMY1B   RBMY1D   RBMY1E   RBMY1F   RPS4Y1   RPS4Y2   SRY   TBL1Y   TGIF2LY   TMSB4Y   TSPY1   TSPY10   TSPY2   TSPY3   TSPY4   TSPY8   TTTY1   TTTY10   TTTY11   TTTY12   TTTY13   TTTY13B   TTTY14   TTTY15   TTTY16   TTTY18   TTTY19   TTTY1B   TTTY2   TTTY20   TTTY21   TTTY21B   TTTY22   TTTY23   TTTY23B   TTTY2B   TTTY5   TTTY6B   TTTY7   TTTY7B   TTTY8   TTTY8B   TTTY9A   TTTY9B   USP9Y   UTY   VCY   VCY1B   XKRY   XKRY2   ZFY   ZFY-AS1  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000024.10:g.(?_2786811)_(22358529_?)dup
NC_000024.9:g.(?_2654852)_(24504676_?)dup
NC_000024.8:g.(?_2714852)_(22914064_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh38Y2,786,811 - 22,358,529CLINVAR
GRCh37Y2,654,852 - 24,504,676CLINVAR
Build 36Y2,714,852 - 22,914,064CLINVAR
Cytogenetic MapYYp11.2-q11.223CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 8618001
Created: 2014-05-13
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.