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Variant : CV158506 (GRCh38/hg38 3q27.3-28(chr3:187521625-188779207)x1) Homo sapiens

Symbol: CV158506
Name: GRCh38/hg38 3q27.3-28(chr3:187521625-188779207)x1
Condition: See cases [RCV000137821]
Clinical Significance: uncertain significance
Last Evaluated: 12/16/2011
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: BCL6   FLJ42393   LINC01991   LPP   LPP-AS1   LPP-AS2   MIR28   RTP2   SST  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000003.12:g.(?_187521625)_(188779207_?)del
NC_000003.11:g.(?_187239413)_(188496995_?)del
NC_000003.10:g.(?_188722107)_(189979689_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh383187,521,625 - 188,779,207CLINVAR
GRCh373187,239,413 - 188,496,995CLINVAR
Build 363188,722,107 - 189,979,689CLINVAR
Cytogenetic Map33q27.3-28CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9485373
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-01-14
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.