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Variant : CV164641 (GRCh38/hg38 Yq11.223(chrY:21568533-22490845)x0) Homo sapiens

Symbol: CV164641
Name: GRCh38/hg38 Yq11.223(chrY:21568533-22490845)x0
Condition: See cases [RCV000142954]
Clinical Significance: likely benign
Last Evaluated: 09/04/2012
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: PRY   PRY2   RBMY1D   RBMY1E   RBMY1F   RBMY1J   TTTY13   TTTY5   TTTY6   TTTY6B  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000024.10:g.(?_21568533)_(22490845_?)del
NC_000024.9:g.(?_23730419)_(24636992_?)del
NC_000024.8:g.(?_22139807)_(23046380_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh38Y21,568,533 - 22,490,845CLINVAR
GRCh37Y23,730,419 - 24,636,992CLINVAR
Build 36Y22,139,807 - 23,046,380CLINVAR
Cytogenetic MapYYq11.223CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9490552
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.