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Variant : CV556148 (GRCh37/hg19 Yq11.222-11.223(chrY:20618887-24820716)x0) Homo sapiens

Symbol: CV556148
Name: GRCh37/hg19 Yq11.222-11.223(chrY:20618887-24820716)x0
Condition: not provided [RCV000684439]
Clinical Significance: likely benign
Last Evaluated: 01/05/2018
Review Status: no assertion criteria provided
Related Genes: EIF1AY   HSFY1   HSFY2   KDM5D   PRORY   PRY   PRY2   RBMY1A1   RBMY1B   RBMY1D   RBMY1E   RBMY1F   RBMY1J   RPS4Y2   TTTY10   TTTY13   TTTY14   TTTY5   TTTY6   TTTY6B   TTTY9A   TTTY9B  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37Y20,618,887 - 24,820,716CLINVAR
Cytogenetic MapYYq11.222-11.223CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13798723
Created: 2018-10-09
Species: Homo sapiens
Last Modified: 2020-05-26
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.