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Variant : CV161090 (GRCh38/hg38 15q15.1(chr15:41697762-42489559)x3) Homo sapiens

Symbol: CV161090
Name: GRCh38/hg38 15q15.1(chr15:41697762-42489559)x3
Condition: See cases [RCV000140056]
Clinical Significance: uncertain significance
Last Evaluated: 11/27/2012
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: CAPN3   EHD4   EHD4-AS1   GANC   JMJD7   JMJD7-PLA2G4B   MAPKBP1   MGA   MIR4310   MIR627   PLA2G4B   PLA2G4D   PLA2G4E   PLA2G4E-AS1   PLA2G4F   SPTBN5   TMEM87A   VPS39   ZNF106  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000015.10:g.(?_41697762)_(42489559_?)dup
NC_000015.9:g.(?_41989960)_(42781757_?)dup
NC_000015.8:g.(?_39777252)_(40569049_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh381541,697,762 - 42,489,559CLINVAR
GRCh371541,989,960 - 42,781,757CLINVAR
Build 361539,777,252 - 40,569,049CLINVAR
Cytogenetic Map1515q15.1CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9487586
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2019-08-06
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.