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Variant : CV164311 (GRCh38/hg38 3p26.3(chr3:190587-608819)x1) Homo sapiens

Symbol: CV164311
Name: GRCh38/hg38 3p26.3(chr3:190587-608819)x1
Condition: See cases [RCV000142624]
Clinical Significance: uncertain significance
Last Evaluated: 02/11/2011
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: CHL1   CHL1-AS1   CHL1-AS2   LINC01266  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000003.12:g.(?_190587)_(608819_?)del
NC_000003.11:g.(?_232270)_(650502_?)del
NC_000003.10:g.(?_207270)_(625502_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh383190,587 - 608,819CLINVAR
GRCh373232,270 - 650,502CLINVAR
Build 363207,270 - 625,502CLINVAR
Cytogenetic Map33p26.3CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9490222
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.