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Variant : CV161736 (GRCh38/hg38 3q27.3-28(chr3:187897470-188570860)x3) Homo sapiens

Symbol: CV161736
Name: GRCh38/hg38 3q27.3-28(chr3:187897470-188570860)x3
Condition: See cases [RCV000140661]
Clinical Significance: uncertain significance
Last Evaluated: 12/10/2012
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: FLJ42393   LINC01991   LPP   LPP-AS1   LPP-AS2  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000003.12:g.(?_187897470)_(188570860_?)dup
NC_000003.11:g.(?_187615258)_(188288648_?)dup
NC_000003.10:g.(?_189097952)_(189771342_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh383187,897,470 - 188,570,860CLINVAR
GRCh373187,615,258 - 188,288,648CLINVAR
Build 363189,097,952 - 189,771,342CLINVAR
Cytogenetic Map33q27.3-28CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9488191
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.