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Variant : CV156096 (GRCh38/hg38 3p26.3(chr3:190813-2045586)x3) Homo sapiens

Symbol: CV156096
Name: GRCh38/hg38 3p26.3(chr3:190813-2045586)x3
Condition: See cases [RCV000135649]
Clinical Significance: uncertain significance
Last Evaluated: 01/27/2011
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: CHL1   CHL1-AS1   CHL1-AS2   CNTN6   LINC01266  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000003.12:g.(?_190813)_(2045586_?)dup
NC_000003.11:g.(?_232496)_(2087270_?)dup
NC_000003.10:g.(?_207496)_(2062270_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh383190,813 - 2,045,586CLINVAR
GRCh373232,496 - 2,087,270CLINVAR
Build 363207,496 - 2,062,270CLINVAR
Cytogenetic Map33p26.3CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9483221
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-02-11
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.