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Variant : CV157841 (GRCh38/hg38 3q27.3-28(chr3:187758581-188811242)x1) Homo sapiens

Symbol: CV157841
Name: GRCh38/hg38 3q27.3-28(chr3:187758581-188811242)x1
Condition: See cases [RCV000137173]
Clinical Significance: uncertain significance
Last Evaluated: 12/22/2010
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: FLJ42393   LINC01991   LPP   LPP-AS1   LPP-AS2   MIR28  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000003.12:g.(?_187758581)_(188811242_?)del
NC_000003.11:g.(?_187476369)_(188529030_?)del
NC_000003.10:g.(?_188959063)_(190011724_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh383187,758,581 - 188,811,242CLINVAR
GRCh373187,476,369 - 188,529,030CLINVAR
Build 363188,959,063 - 190,011,724CLINVAR
Cytogenetic Map33q27.3-28CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9484732
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-01-07
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.