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Variant : CV162972 (GRCh38/hg38 3p26.3(chr3:20213-1755128)x1) Homo sapiens

Symbol: CV162972
Name: GRCh38/hg38 3p26.3(chr3:20213-1755128)x1
Condition: See cases [RCV000141686]
Clinical Significance: likely benign|uncertain significance
Last Evaluated: 07/18/2014
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: CHL1   CHL1-AS1   CHL1-AS2   CNTN6   LINC01266   LINC01986  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000003.12:g.(?_20213)_(1755128_?)del
NC_000003.11:g.(?_61891)_(1796812_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh38320,213 - 1,755,128CLINVAR
GRCh37361,891 - 1,796,812CLINVAR
Build 36336,891 - 1,771,812CLINVAR
Cytogenetic Map33p26.3CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9489211
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.