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Variant : CV163106 (GRCh38/hg38 Yp11.2(chrY:9688291-10236356)x2) Homo sapiens

Symbol: CV163106
Name: GRCh38/hg38 Yp11.2(chrY:9688291-10236356)x2
Condition: See cases [RCV000141778]
Clinical Significance: likely benign
Last Evaluated: 05/14/2013
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: TTTY1   TTTY2   TTTY21   TTTY22   TTTY23   TTTY7B   TTTY8  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000024.10:g.(?_9688291)_(10236356_?)dup
NC_000024.9:g.(?_9525900)_(10073965_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh38Y9,688,291 - 10,236,356CLINVAR
GRCh37Y9,525,900 - 10,073,965CLINVAR
Build 36Y10,135,900 - 10,683,965CLINVAR
Cytogenetic MapYYp11.2CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9489301
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.