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Variant : CV247384 (GRCh37/hg19 Yp11.2(chrY:9417393-9882301)x2) Homo sapiens

Symbol: CV247384
Name: GRCh37/hg19 Yp11.2(chrY:9417393-9882301)x2
Condition: See cases [RCV000239405]
Clinical Significance: uncertain significance
Last Evaluated: 06/14/2016
Review Status: criteria provided, single submitter
Related Genes: TTTY1   TTTY2   TTTY21   TTTY22   TTTY23   TTTY7B   TTTY8  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37Y9,417,393 - 9,882,301CLINVAR
Cytogenetic MapYYp11.2CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 11531144
Created: 2016-09-01
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.