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Variant : CV158289 (GRCh38/hg38 Yp11.2(chrY:5874108-7106335)x0) Homo sapiens

Symbol: CV158289
Name: GRCh38/hg38 Yp11.2(chrY:5874108-7106335)x0
Condition: See cases [RCV000137611]
Clinical Significance: likely benign
Last Evaluated: 02/25/2011
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: AMELY   FAM197Y9   LINC00280   TBL1Y   TSPY2   TTTY1B   TTTY21B   TTTY23B   TTTY2B   TTTY7   TTTY8B  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000024.10:g.(?_5874108)_(7106335_?)del
NC_000024.9:g.(?_5742149)_(6974376_?)del
NC_000024.8:g.(?_5802149)_(7034376_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh38Y5,874,108 - 7,106,335CLINVAR
GRCh37Y5,742,149 - 6,974,376CLINVAR
Build 36Y5,802,149 - 7,034,376CLINVAR
Cytogenetic MapYYp11.2CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9485164
Created: 2014-09-09
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.