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Items: 1 to 20 of 368

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5964078insertion1nstd209human GRCh38 chr1: 175,112,598-175,112,598 , GRCh37.p13 chr1: 175,081,734-175,081,734 TNN
    nsv5952947insertion1nstd209human GRCh38 chr1: 175,103,565-175,103,565 , GRCh37.p13 chr1: 175,072,701-175,072,701 TNN
    nsv5882727copy number variation1nstd209human GRCh38 chr1: 175,101,007-175,107,139 , GRCh37.p13 chr1: 175,070,143-175,076,275 TNN
    nsv5878085copy number variation1nstd209human GRCh38 chr1: 175,097,859-175,097,981 , GRCh37.p13 chr1: 175,066,995-175,067,117 TNN
    nsv5872800copy number variation1nstd209human GRCh38 chr1: 175,101,997-175,102,115 , GRCh37.p13 chr1: 175,071,133-175,071,251 TNN
    nsv5872098copy number variation1nstd209human GRCh38 chr1: 175,122,457-175,122,508 , GRCh37.p13 chr1: 175,091,593-175,091,644 TNN
    nsv5868791copy number variation1nstd209human GRCh38 chr1: 175,105,144-175,105,321 , GRCh37.p13 chr1: 175,074,280-175,074,457 TNN
    nsv5828642copy number variation5nstd209human GRCh38 chr1: 175,101,849-175,107,508 , GRCh37.p13 chr1: 175,070,985-175,076,644 TNN
    nsv5727988mobile element insertion2nstd211human GRCh38 chr1: 175,103,579-175,103,579 , GRCh37.p13 chr1: 175,072,715-175,072,715 TNN
    nsv5583796copy number variation1nstd207human GRCh38 chr1: 175,101,924-175,108,081 , GRCh37.p13 chr1: 175,071,060-175,077,217 TNN
    nsv5570625copy number variation1nstd207human GRCh38 chr1: 175,122,455-175,122,506 , GRCh37.p13 chr1: 175,091,591-175,091,642 TNN
    nsv5432577copy number variation1nstd206human GRCh38 chr1: 175,122,457-175,122,510 , GRCh37.p13 chr1: 175,091,593-175,091,646 TNN
    nsv5430749copy number variation1nstd206human GRCh38 chr1: 175,062,370-175,145,289 , GRCh37.p13 chr1: 175,031,506-175,114,425 TNN
    nsv5428476copy number variation1nstd206human GRCh38 chr1: 175,100,587-175,108,440 , GRCh37.p13 chr1: 175,069,723-175,077,576 TNN
    nsv5425764copy number variation1nstd206human GRCh38 chr1: 175,097,579-175,098,461 , GRCh37.p13 chr1: 175,066,715-175,067,597 TNN
    nsv5407372mobile element insertion1nstd206human GRCh38 chr1: 175,103,579-175,103,617 , GRCh37.p13 chr1: 175,072,715-175,072,753 TNN
    nsv5381285copy number variation2nstd102humanUncertain significance GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699 , DCST1, 2428 more genes
    nsv5347307translocation1nstd200human GRCh38 chr1: 175,122,510-175,122,510 , GRCh38 chr1: 175,122,457-175,122,457 , GRCh37.p13 chr1: 175,091,646-175,091,646 , GRCh37.p13 chr1: 175,091,593-175,091,593 TNN
    nsv5333093translocation1nstd200human GRCh37 chr1: 175,091,646-175,091,646 , GRCh37 chr1: 175,091,593-175,091,593 , GRCh38.p12 chr1: 175,122,457-175,122,457 , GRCh38.p12 chr1: 175,122,510-175,122,510 TNN
    nsv5329088translocation1nstd204human GRCh38.p13 chr1: 175,122,510-175,122,510 , GRCh38.p13 chr1: 175,122,457-175,122,457 , GRCh37.p13 chr1: 175,091,646-175,091,646 , GRCh37.p13 chr1: 175,091,593-175,091,593 TNN
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