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Variant : CV160965 (GRCh38/hg38 Yq11.221-12(chrY:16311571-57190586)x0) Homo sapiens

Symbol: CV160965
Name: GRCh38/hg38 Yq11.221-12(chrY:16311571-57190586)x0
Condition: See cases [RCV000139941]
Clinical Significance: pathogenic
Last Evaluated: 03/26/2013
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   XKRY   XKRY2  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000024.10:g.(?_16311571)_(57190586_?)del
NC_000024.9:g.(?_18423451)_(59336737_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh38Y16,311,571 - 57,190,586CLINVAR
GRCh37Y18,423,451 - 59,336,737CLINVAR
Build 36Y16,932,845 - 57,746,125CLINVAR
Cytogenetic MapYYq11.221-12CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9487471
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2019-12-03
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.