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Items: 1 to 20 of 180

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5664251insertion1nstd207human GRCh38 chr19: 55,134,791-55,134,791 , GRCh37.p13 chr19: 55,646,159-55,646,159 TNNT1
    nsv5649928insertion1nstd207human GRCh38 chr19: 55,137,506-55,137,506 , GRCh37.p13 chr19: 55,648,874-55,648,874 TNNT1
    nsv5649568insertion1nstd207human GRCh38 chr19: 55,137,512-55,137,512 , GRCh37.p13 chr19: 55,648,880-55,648,880 TNNT1
    nsv5600476copy number variation1nstd207human GRCh38 chr19: 55,147,345-55,147,417 , GRCh37.p13 chr19: 55,658,713-55,658,785 TNNT1
    nsv5180010mobile element insertion1nstd203human GRCh38 chr19: 55,142,277-55,142,292 , GRCh37.p13 chr19: 55,653,645-55,653,660 TNNT1
    nsv5024962copy number variation1nstd200human GRCh38 chr19: 55,130,133-55,134,584 , GRCh37.p13 chr19: 55,641,501-55,645,952 TNNT1
    nsv4865344copy number variation1nstd200human GRCh37 chr19: 55,641,501-55,645,952 , GRCh38.p12 chr19: 55,130,133-55,134,584 TNNT1
    nsv4760524insertion1nstd199human GRCh37 chr19: 55,648,824-55,648,824 , GRCh38.p12 chr19: 55,137,456-55,137,456 TNNT1
    nsv4753422insertion1nstd199human GRCh37 chr19: 55,646,040-55,646,040 , GRCh38.p12 chr19: 55,134,672-55,134,672 TNNT1
    nsv4736192copy number variation1nstd199human GRCh37 chr19: 55,658,719-55,658,792 , GRCh38.p12 chr19: 55,147,351-55,147,424 TNNT1
    nsv4730034copy number variation1nstd102humanUncertain significance GRCh37 chr19: 54,334,195-56,434,037 , GRCh38.p12 chr19: 53,830,941-55,922,671 , GRCh38.p12 chr19|NT_187693.1: 1-1,066,800 , GRCh38.p12 chr19|NW_003571057.2: 1-1,091,841 , GRCh38.p12 chr19|NW_003571058.2: 1-1,066,390 , GRCh38.p12 chr19|NW_003571056.2: 1-1,064,304 KIR3DP1, NLRP9, 133 more genes
    nsv4729755copy number variation1nstd102humanPathogenic GRCh37 chr19: 48,463,931-57,095,254 , GRCh38.p12 chr19: 47,960,674-56,583,886 SIGLEC5, MED25, 574 more genes
    nsv4682620copy number variation1nstd102humanUncertain significance GRCh37 chr19: 55,652,241-55,663,295 , GRCh38.p12 chr19: 55,140,873-55,151,927 TNNI3, TNNT1
    nsv4671731copy number variation1nstd186human GRCh37 chr19: 55,656,501-55,661,200 , GRCh38.p12 chr19: 55,145,133-55,149,832 TNNI3, TNNT1
    nsv4631645copy number variation1nstd183human GRCh37 chr19: 55,658,049-55,658,106 , GRCh38.p12 chr19: 55,146,681-55,146,738 TNNT1
    nsv4628083copy number variation1nstd183human GRCh37 chr19: 55,656,501-55,661,200 , GRCh38.p12 chr19: 55,145,133-55,149,832 TNNT1, TNNI3
    nsv4457750copy number variation1nstd102humanUncertain significance GRCh37 chr19: 55,508,564-55,665,523 , GRCh38.p12 chr19|NW_003571056.2: 977,182-1,064,304 , GRCh38.p12 chr19|NT_187693.1: 979,678-1,066,800 , GRCh38.p12 chr19|NW_003571054.1: 900,594-987,716 , GRCh38.p12 chr19: 54,997,196-55,154,155 , GRCh38.p12 chr19|NW_003571061.2: 709,357-796,479 , GRCh38.p12 chr19|NW_003571057.2: 1,004,719-1,091,841 , GRCh38.p12 chr19|NW_003571059.2: 915,561-1,002,683 , GRCh38.p12 chr19|NW_003571060.1: 899,978-987,100 , GRCh38.p12 chr19|NW_003571058.2: 979,268-1,066,390 , GRCh38.p12 chr19|NW_003571055.2: 642,398-729,520 TNNI3, TNNT1, 7 more genes
    nsv4454487copy number variation1nstd102humanPathogenic GRCh38 chr19: 55,140,873-55,147,167 , GRCh37 chr19: 55,652,241-55,658,535 TNNT1
    nsv4452266copy number variation2nstd102humanUncertain significance GRCh38 chr19: 55,132,905-55,256,909 , GRCh37 chr19: 55,644,273-55,768,277 DNAAF3, MIR6802, 9 more genes
    nsv4451628copy number variation1nstd102humanPathogenic GRCh37 chr19: 55,652,231-55,663,305 , GRCh38 chr19: 55,140,863-55,151,937 TNNI3, TNNT1
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