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Variant : CV556138 (GRCh37/hg19 Yq11.23(chrY:26241299-27723547)x0) Homo sapiens

Symbol: CV556138
Name: GRCh37/hg19 Yq11.23(chrY:26241299-27723547)x0
Condition: not provided [RCV000684429]
Clinical Significance: uncertain significance
Last Evaluated: 11/01/2017
Review Status: no assertion criteria provided
Related Genes: BPY2B   BPY2C   DAZ3   DAZ4   TTTY17B   TTTY17C   TTTY4B   TTTY4C  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37Y26,241,299 - 27,723,547CLINVAR
Cytogenetic MapYYq11.23CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13798665
Created: 2018-10-09
Species: Homo sapiens
Last Modified: 2020-02-20
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.