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Variant : CV164270 (GRCh38/hg38 3p26.3(chr3:52266-1091944)x1) Homo sapiens

Symbol: CV164270
Name: GRCh38/hg38 3p26.3(chr3:52266-1091944)x1
Condition: See cases [RCV000142583]
Clinical Significance: uncertain significance
Last Evaluated: 12/22/2010
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.(?_52266)_(1091944_?)del
NC_000003.11:g.(?_93949)_(1133628_?)del
NC_000003.10:g.(?_68949)_(1108628_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh38352,266 - 1,091,944CLINVAR
GRCh37393,949 - 1,133,628CLINVAR
Build 36368,949 - 1,108,628CLINVAR
Cytogenetic Map33p26.3CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9490181
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-02-20
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.