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Items: 1 to 20 of 632

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112765copy number variation1nstd102humanPathogenic GRCh37 chr10: 118,247,181-135,435,319 , GRCh38.p12 chr10: 116,487,669-133,621,815 STK32C, LOC105378542, 266 more genes
    nsv5980446copy number variation1nstd102humanPathogenic GRCh37 chr10: 122,785,023-135,457,222 , GRCh38.p12 chr10: 121,025,510-133,643,718 LINC02641, CFAP46, 194 more genes
    nsv5977530insertion1nstd209human GRCh38 chr10: 133,397,401-133,397,401 , GRCh37.p13 chr10: 135,210,905-135,210,905 MTG1
    nsv5926289copy number variation1nstd209human GRCh38 chr10: 133,371,188-133,471,140 , GRCh37.p13 chr10: 135,184,692-135,284,644 , ECHS1, 6 more genes
    nsv5859471copy number variation1nstd209human GRCh38 chr10: 133,390,536-133,396,835 , GRCh37.p13 chr10: 135,204,040-135,210,339 PAOX, MTG1
    nsv5856182copy number variation1nstd209human GRCh38 chr10: 133,390,886-133,413,664 , GRCh37.p13 chr10: 135,204,390-135,227,168 MTG1, PAOX
    nsv5730254mobile element insertion2nstd211human GRCh38 chr10: 133,397,418-133,397,418 , GRCh37.p13 chr10: 135,210,922-135,210,922 MTG1
    nsv5710312mobile element insertion2nstd211human GRCh38 chr10: 133,411,177-133,411,177 , GRCh37.p13 chr10: 135,224,681-135,224,681 MTG1
    nsv5672526copy number variation1nstd102humanPathogenic GRCh37 chr10: 127,548,166-135,440,251 , GRCh38.p12 chr10: 125,859,597-133,626,747 LINC00601, RPL5P28, 110 more genes
    nsv5660332insertion1nstd207human GRCh38 chr10: 133,415,974-133,415,974 , GRCh37.p13 chr10: 135,229,478-135,229,478 MTG1
    nsv5659811insertion1nstd207human GRCh38 chr10: 133,397,401-133,397,401 , GRCh37.p13 chr10: 135,210,905-135,210,905 MTG1
    nsv5647060insertion1nstd207human GRCh38 chr10: 133,403,044-133,403,044 , GRCh37.p13 chr10: 135,216,548-135,216,548 MTG1
    nsv5598932copy number variation1nstd207human GRCh38 chr10: 133,403,129-133,403,340 , GRCh37.p13 chr10: 135,216,633-135,216,844 MTG1
    nsv5588082copy number variation1nstd207human GRCh38 chr10: 133,403,288-133,403,340 , GRCh37.p13 chr10: 135,216,792-135,216,844 MTG1
    nsv5504922copy number variation1nstd206human GRCh38 chr10: 133,392,407-133,392,687 , GRCh37.p13 chr10: 135,205,911-135,206,191 MTG1
    nsv5501586copy number variation1nstd206human GRCh38 chr10: 133,401,130-133,457,130 , GRCh37.p13 chr10: 135,214,634-135,270,634 MTG1, SCART1, 2 more genes
    nsv5413667mobile element insertion1nstd206human GRCh38 chr10: 133,411,177-133,411,228 , GRCh37.p13 chr10: 135,224,681-135,224,732 MTG1
    nsv5381769copy number variation1nstd102humanPathogenic GRCh37 chr10: 129,483,682-135,434,178 , GRCh38.p12 chr10: 127,685,418-133,620,674 DPYSL4, LINC02667, 88 more genes
    nsv5354636translocation1nstd200human GRCh38 chr10: 133,392,407-133,392,407 , GRCh38 chr10: 133,392,687-133,392,687 , GRCh37.p13 chr10: 135,206,191-135,206,191 , GRCh37.p13 chr10: 135,205,911-135,205,911 MTG1
    nsv5318586copy number variation1nstd204human GRCh37.p13 chr10: 135,203,636-135,207,666 , GRCh38.p13 chr10: 133,390,132-133,394,162 MTG1, PAOX
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