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Variant : CV556149 (GRCh37/hg19 Yq11.223-11.23(chrY:24073794-28799937)x0) Homo sapiens

Symbol: CV556149
Name: GRCh37/hg19 Yq11.223-11.23(chrY:24073794-28799937)x0
Condition: not provided [RCV000684440]
Clinical Significance: pathogenic
Last Evaluated: 10/25/2017
Review Status: no assertion criteria provided
Related Genes: BPY2   BPY2B   BPY2C   CDY1   DAZ1   DAZ2   DAZ3   DAZ4   PRY   PRY2   RBMY1F   RBMY1J   TTTY17A   TTTY17B   TTTY17C   TTTY3   TTTY3B   TTTY4   TTTY4B   TTTY4C   TTTY5   TTTY6   TTTY6B  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37Y24,073,794 - 28,799,937CLINVAR
Cytogenetic MapYYq11.223-11.23CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13798676
Created: 2018-10-09
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.