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Variant : CV164456 (GRCh38/hg38 Yq11.222-11.223(chrY:18664321-22358529)x2) Homo sapiens

Symbol: CV164456
Name: GRCh38/hg38 Yq11.222-11.223(chrY:18664321-22358529)x2
Condition: See cases [RCV000142769]
Clinical Significance: uncertain significance
Last Evaluated: 12/22/2010
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: EIF1AY   HSFY2   KDM5D   PRORY   PRY2   RBMY1A1   RBMY1B   RBMY1D   RBMY1E   RBMY1F   RPS4Y2   TTTY10   TTTY13   TTTY14   TTTY5   TTTY6B   TTTY9A  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000024.10:g.(?_18664321)_(22358529_?)dup
NC_000024.9:g.(?_20826207)_(24504676_?)dup
NC_000024.8:g.(?_19285595)_(22914064_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh38Y18,664,321 - 22,358,529CLINVAR
GRCh37Y20,826,207 - 24,504,676CLINVAR
Build 36Y19,285,595 - 22,914,064CLINVAR
Cytogenetic MapYYq11.222-11.223CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9490367
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-05-19
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.