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Variant : CV71916 (GRCh38/hg38 Yp11.2(chrY:2786811-9007152)x2) Homo sapiens

Symbol: CV71916
Name: GRCh38/hg38 Yp11.2(chrY:2786811-9007152)x2
Condition: See cases [RCV000051006]
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   FAM197Y9   LINC00278   LINC00279   LINC00280   MIR9985   PCDH11Y   RPS4Y1   SRY   TBL1Y   TGIF2LY   TSPY2   TTTY11   TTTY12   TTTY16   TTTY18   TTTY19   TTTY1B   TTTY21B   TTTY23B   TTTY2B   TTTY7   TTTY8B   ZFY   ZFY-AS1  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000024.10:g.(?_2786811)_(9007152_?)dup
NC_000024.9:g.(?_2654852)_(8875193_?)dup
NC_000024.8:g.(?_2714852)_(8935193_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh38Y2,786,811 - 9,007,152CLINVAR
GRCh37Y2,654,852 - 8,875,193CLINVAR
Build 36Y2,714,852 - 8,935,193CLINVAR
Cytogenetic MapYYp11.2CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 8618057
Created: 2014-05-13
Species: Homo sapiens
Last Modified: 2020-05-26
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.