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Variant : CV165380 (GRCh38/hg38 3p26.3-26.2(chr3:20213-3244317)x1) Homo sapiens

Symbol: CV165380
Name: GRCh38/hg38 3p26.3-26.2(chr3:20213-3244317)x1
Condition: See cases [RCV000143693]
Clinical Significance: uncertain significance
Last Evaluated: 12/03/2013
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: CHL1   CHL1-AS1   CHL1-AS2   CNTN4   CNTN4-AS1   CNTN4-AS2   CNTN6   CRBN   IL5RA   LINC01266   LINC01986   TRNT1  
Variant Type: copy number loss (SO:0001743)
Evidence: clinical testing
HGVS Name(s): NC_000003.12:g.(?_20213)_(3244317_?)del
Human AssemblyChrPosition (strand)Source
GRCh38320,213 - 3,244,317CLINVAR
GRCh37361,891 - 3,286,001CLINVAR
Build 36336,891 - 3,261,001CLINVAR
Cytogenetic Map33p26.3-26.2CLINVAR

References - uncurated

Additional Information

External Database Links
CRRD Object Information
CRRD ID: 9491291
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-02-20
Status: ACTIVE


RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.