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Variant : CV156373 (GRCh38/hg38 Yq11.221-12(chrY:15631816-57211010)x0) Homo sapiens

Symbol: CV156373
Name: GRCh38/hg38 Yq11.221-12(chrY:15631816-57211010)x0
Condition: See cases [RCV000135882]
Clinical Significance: pathogenic
Last Evaluated: 02/16/2011
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: BPY2   BPY2B   BPY2C   CDY1   CDY1B   CDY2A   CDY2B   DAZ1   DAZ2   DAZ3   DAZ4   EIF1AY   FAM224A   FAM224B   FAM41AY1   FAM41AY2   HSFY1   HSFY2   IL9R   KDM5D   PRORY   PRY   PRY2   RBMY1A1   RBMY1B   RBMY1D   RBMY1E   RBMY1F   RBMY1J   RPS4Y2   SPRY3   TTTY10   TTTY13   TTTY14   TTTY17A   TTTY17B   TTTY17C   TTTY3   TTTY3B   TTTY4   TTTY4B   TTTY4C   TTTY5   TTTY6   TTTY6B   TTTY9A   TTTY9B   VAMP7   WASIR1   XKRY   XKRY2  
Variant Type: copy number loss (SO:0001743)
Evidence: clinical testing
HGVS Name(s): NC_000024.10:g.(?_15631816)_(57211010_?)del
Human AssemblyChrPosition (strand)Source
GRCh38Y15,631,816 - 57,211,010CLINVAR
GRCh37Y17,743,696 - 59,357,161CLINVAR
Build 36Y16,253,090 - 57,766,549CLINVAR
Cytogenetic MapYYq11.221-12CLINVAR

References - uncurated

Additional Information

External Database Links
CRRD Object Information
CRRD ID: 9483448
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-03-24
Status: ACTIVE


RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.