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Variant : CV161632 (GRCh38/hg38 3p26.3(chr3:190813-213696)x3) Homo sapiens

Symbol: CV161632
Name: GRCh38/hg38 3p26.3(chr3:190813-213696)x3
Condition: See cases [RCV000140566]
Clinical Significance: benign
Last Evaluated: 04/30/2011
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: CHL1   CHL1-AS2  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000003.12:g.(?_190813)_(213696_?)dup
NC_000003.11:g.(?_232496)_(255379_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh383190,813 - 213,696CLINVAR
GRCh373232,496 - 255,379CLINVAR
Build 363207,496 - 230,379CLINVAR
Cytogenetic Map33p26.3CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9488096
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.