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Pathways
Variants search result for Homo sapiens
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1 records found for search term 7356110
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
9491364CV165453copy number gainGRCh38/hg38 3p26.1-25.1(chr3:7356110-14360442)x3See cases [RCV000143766]pathogenic3735611014360442Humanname