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Variant : CV155227 (GRCh38/hg38 Yp11.2-q11.23(chrY:6270281-26463761)x0) Homo sapiens

Symbol: CV155227
Name: GRCh38/hg38 Yp11.2-q11.23(chrY:6270281-26463761)x0
Condition: See cases [RCV000134844]
Clinical Significance: pathogenic
Last Evaluated: 09/30/2010
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: AMELY   BPY2   BPY2B   BPY2C   CDY1   CDY1B   CDY2A   CDY2B   DAZ1   DAZ2   DAZ3   DAZ4   DDX3Y   EIF1AY   FAM197Y1   FAM197Y2   FAM197Y3   FAM197Y4   FAM197Y5   FAM197Y6   FAM197Y7   FAM197Y8   FAM224A   FAM224B   FAM41AY1   FAM41AY2   HSFY1   HSFY2   KDM5D   LINC00279   LINC00280   MIR12120   NLGN4Y   NLGN4Y-AS1   PRORY   PRY   PRY2   RBMY1A1   RBMY1B   RBMY1D   RBMY1E   RBMY1F   RBMY1J   RPS4Y2   TBL1Y   TMSB4Y   TSPY1   TSPY10   TSPY3   TSPY4   TSPY8   TTTY1   TTTY10   TTTY11   TTTY12   TTTY13   TTTY13B   TTTY14   TTTY15   TTTY16   TTTY17A   TTTY17B   TTTY17C   TTTY18   TTTY19   TTTY1B   TTTY2   TTTY20   TTTY21   TTTY21B   TTTY22   TTTY23   TTTY2B   TTTY3   TTTY3B   TTTY4   TTTY4B   TTTY4C   TTTY5   TTTY6   TTTY6B   TTTY7   TTTY7B   TTTY8   TTTY8B   TTTY9A   TTTY9B   USP9Y   UTY   VCY   VCY1B   XKRY   XKRY2  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000024.10:g.(?_6270281)_(26463761_?)del
NC_000024.9:g.(?_6138322)_(28609908_?)del
NC_000024.8:g.(?_6198322)_(27019296_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh38Y6,270,281 - 26,463,761CLINVAR
GRCh37Y6,138,322 - 28,609,908CLINVAR
Build 36Y6,198,322 - 27,019,296CLINVAR
Cytogenetic MapYYp11.2-q11.23CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9482421
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.