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Variant : CV608772 (GRCh37/hg19 Yq11.223-11.23(chrY:24461432-28742675)x3) Homo sapiens

Symbol: CV608772
Name: GRCh37/hg19 Yq11.223-11.23(chrY:24461432-28742675)x3
Condition: not provided [RCV000754072]
Clinical Significance: benign
Last Evaluated: 10/01/2012
Review Status: no assertion criteria provided
Related Genes: BPY2   BPY2B   BPY2C   CDY1   DAZ1   DAZ2   DAZ3   DAZ4   PRY   RBMY1J   TTTY17A   TTTY17B   TTTY17C   TTTY3   TTTY3B   TTTY4   TTTY4B   TTTY4C   TTTY6  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37Y24,461,432 - 28,742,675CLINVAR
Cytogenetic MapYYq11.223-11.23CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14350986
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2020-02-11
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.