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Variant : CV380855 (GRCh37/hg19 Yq11.223-12(chrY:24108372-59358798)x0) Homo sapiens

Symbol: CV380855
Name: GRCh37/hg19 Yq11.223-12(chrY:24108372-59358798)x0
Condition: See cases [RCV000447015]
Clinical Significance: pathogenic
Last Evaluated:
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   WASIR1  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37Y24,108,372 - 59,358,798CLINVAR
Cytogenetic MapYYq11.223-12CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 12851735
Created: 2017-04-11
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.