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Variant : CV164349 (GRCh38/hg38 Yq11.223(chrY:21034147-22358529)x2) Homo sapiens

Symbol: CV164349
Name: GRCh38/hg38 Yq11.223(chrY:21034147-22358529)x2
Condition: See cases [RCV000142662]
Clinical Significance: uncertain significance
Last Evaluated: 12/22/2010
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: PRORY   PRY2   RBMY1A1   RBMY1B   RBMY1D   RBMY1E   RBMY1F   TTTY13   TTTY5   TTTY6B  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000024.10:g.(?_21034147)_(22358529_?)dup
NC_000024.9:g.(?_23196033)_(24504676_?)dup
NC_000024.8:g.(?_21605421)_(22914064_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh38Y21,034,147 - 22,358,529CLINVAR
GRCh37Y23,196,033 - 24,504,676CLINVAR
Build 36Y21,605,421 - 22,914,064CLINVAR
Cytogenetic MapYYq11.223CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9490260
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-05-26
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.