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Variant : CV159503 (GRCh38/hg38 Yp11.2(chrY:6234800-8705376)x2) Homo sapiens

Symbol: CV159503
Name: GRCh38/hg38 Yp11.2(chrY:6234800-8705376)x2
Condition: See cases [RCV000138714]
Clinical Significance: likely benign
Last Evaluated: 06/11/2012
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: AMELY   FAM197Y9   LINC00279   LINC00280   TBL1Y   TSPY2   TTTY12   TTTY16   TTTY18   TTTY19   TTTY1B   TTTY21B   TTTY23B   TTTY2B   TTTY7   TTTY8B  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000024.10:g.(?_6234800)_(8705376_?)dup
NC_000024.9:g.(?_6102841)_(8573417_?)dup
NC_000024.8:g.(?_6162841)_(8633417_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh38Y6,234,800 - 8,705,376CLINVAR
GRCh37Y6,102,841 - 8,573,417CLINVAR
Build 36Y6,162,841 - 8,633,417CLINVAR
Cytogenetic MapYYp11.2CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9486251
Created: 2014-09-09
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.