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Variant : CV161714 (GRCh38/hg38 Yp11.2-q11.222(chrY:2782272-17454794)x2) Homo sapiens

Symbol: CV161714
Name: GRCh38/hg38 Yp11.2-q11.222(chrY:2782272-17454794)x2
Condition: See cases [RCV000140647]
Clinical Significance: pathogenic
Last Evaluated: 12/04/2012
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: AMELY   DDX3Y   FAM197Y1   FAM197Y2   FAM197Y3   FAM197Y4   FAM197Y5   FAM197Y6   FAM197Y7   FAM197Y8   FAM197Y9   LINC00278   LINC00279   LINC00280   MIR12120   MIR9985   NLGN4Y   NLGN4Y-AS1   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   ZFY-AS1  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000024.10:g.(?_2782272)_(17454794_?)dup
NC_000024.9:g.(?_2650313)_(19566674_?)dup
NC_000024.8:g.(?_2710313)_(18076068_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh38Y2,782,272 - 17,454,794CLINVAR
GRCh37Y2,650,313 - 19,566,674CLINVAR
Build 36Y2,710,313 - 18,076,068CLINVAR
Cytogenetic MapYYp11.2-q11.222CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9488177
Created: 2014-09-09
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.