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Variant : CV154012 (GRCh38/hg38 3p26.3(chr3:190813-1155998)x1) Homo sapiens

Symbol: CV154012
Name: GRCh38/hg38 3p26.3(chr3:190813-1155998)x1
Condition: See cases [RCV000133743]
Clinical Significance: uncertain significance
Last Evaluated: 07/01/2013
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: CHL1   CHL1-AS1   CHL1-AS2   CNTN6   LINC01266  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000003.12:g.(?_190813)_(1155998_?)del
NC_000003.11:g.(?_232496)_(1197682_?)del
NC_000003.10:g.(?_207496)_(1172682_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh383190,813 - 1,155,998CLINVAR
GRCh373232,496 - 1,197,682CLINVAR
Build 363207,496 - 1,172,682CLINVAR
Cytogenetic Map33p26.3CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9481328
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.