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Variant : CV158233 (GRCh38/hg38 Yq11.222-12(chrY:18545732-57189762)x0) Homo sapiens

Symbol: CV158233
Name: GRCh38/hg38 Yq11.222-12(chrY:18545732-57189762)x0
Condition: See cases [RCV000137556]
Clinical Significance: pathogenic
Last Evaluated: 02/25/2011
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: BPY2   BPY2B   BPY2C   CDY1   CDY1B   DAZ1   DAZ2   DAZ3   DAZ4   EIF1AY   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  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000024.10:g.(?_18545732)_(57189762_?)del
NC_000024.8:g.(?_19167006)_(57745301_?)del
NC_000024.9:g.(?_20707618)_(59335913_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh38Y18,545,732 - 57,189,762CLINVAR
GRCh37Y20,707,618 - 59,335,913CLINVAR
Build 36Y19,167,006 - 57,745,301CLINVAR
Cytogenetic MapYYq11.222-12CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9485111
Created: 2014-09-09
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.