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Variant : CV436543 (GRCh37/hg19 Yq11.23(chrY:26241299-27699077)x0) Homo sapiens

Symbol: CV436543
Name: GRCh37/hg19 Yq11.23(chrY:26241299-27699077)x0
Condition: See cases [RCV000512320]
Clinical Significance: uncertain significance
Last Evaluated: 08/13/2015
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 - 27,699,077CLINVAR
Cytogenetic MapYYq11.23CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13445285
Created: 2017-11-07
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.