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Variant : CV556144 (GRCh37/hg19 Yq11.223-11.23(chrY:24740855-28321739)x0) Homo sapiens

Symbol: CV556144
Name: GRCh37/hg19 Yq11.223-11.23(chrY:24740855-28321739)x0
Condition: not provided [RCV000684435]
Clinical Significance: pathogenic
Last Evaluated: 08/28/2017
Review Status: no assertion criteria provided
Related Genes: BPY2   BPY2B   BPY2C   CDY1   DAZ1   DAZ2   DAZ3   DAZ4   TTTY17A   TTTY17B   TTTY17C   TTTY3   TTTY3B   TTTY4   TTTY4B   TTTY4C  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37Y24,740,855 - 28,321,739CLINVAR
Cytogenetic MapYYq11.223-11.23CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13798671
Created: 2018-10-09
Species: Homo sapiens
Last Modified: 2019-11-12
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.