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Variant : CV154201 (GRCh38/hg38 9p24.3(chr9:204090-639077)x3) Homo sapiens

Symbol: CV154201
Name: GRCh38/hg38 9p24.3(chr9:204090-639077)x3
Condition: See cases [RCV000133932]
Clinical Significance: benign
Last Evaluated: 05/30/2010
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: DOCK8   DOCK8-AS1   KANK1  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000009.12:g.(?_204090)_(639077_?)dup
NC_000009.11:g.(?_204090)_(639077_?)dup
NC_000009.10:g.(?_194090)_(629077_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh389204,090 - 639,077CLINVAR
GRCh379204,090 - 639,077CLINVAR
Build 369194,090 - 629,077CLINVAR
Cytogenetic Map99p24.3CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9481517
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.