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Variant : CV159007 (GRCh38/hg38 9p24.3(chr9:204104-1457665)x1) Homo sapiens

Symbol: CV159007
Name: GRCh38/hg38 9p24.3(chr9:204104-1457665)x1
Condition: See cases [RCV000138306]
Clinical Significance: uncertain significance
Last Evaluated: 04/16/2012
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: DMRT1   DMRT2   DMRT3   DOCK8   DOCK8-AS1   KANK1   LINC01230  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000009.12:g.(?_204104)_(1457665_?)del
NC_000009.11:g.(?_204104)_(1457665_?)del
NC_000009.10:g.(?_194104)_(1447665_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh389204,104 - 1,457,665CLINVAR
GRCh379204,104 - 1,457,665CLINVAR
Build 369194,104 - 1,447,665CLINVAR
Cytogenetic Map99p24.3CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9485855
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-01-14
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.