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Items: 1 to 20 of 179

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5963002insertion1nstd209human GRCh38 chr1: 152,684,555-152,684,555 , GRCh37.p13 chr1: 152,657,031-152,657,031 LCE2B
    nsv5828238copy number variation1nstd209human GRCh38 chr1: 152,680,309-152,687,730 , GRCh37.p13 chr1: 152,652,785-152,660,206 LCE2B
    nsv5828143copy number variation1nstd209human GRCh38 chr1: 152,674,062-152,685,507 , GRCh37.p13 chr1: 152,646,538-152,657,983 LCE2B, LCE2C
    nsv5690252mobile element insertion2nstd211human GRCh38 chr1: 152,684,570-152,684,570 , GRCh37.p13 chr1: 152,657,046-152,657,046 LCE2B
    nsv5619809insertion1nstd207human GRCh38 chr1: 152,684,555-152,684,555 , GRCh37.p13 chr1: 152,657,031-152,657,031 LCE2B
    nsv5545682insertion1nstd206human GRCh38 chr1: 152,684,570-152,684,613 , GRCh37.p13 chr1: 152,657,046-152,657,089 LCE2B
    nsv5421580copy number variation1nstd206human GRCh38 chr1: 152,489,543-152,734,782 , GRCh37.p13 chr1: 152,462,019-152,707,258 LCE2D, LCE5A, 14 more genes
    nsv5419670copy number variation1nstd206human GRCh38 chr1: 152,676,082-152,687,311 , GRCh37.p13 chr1: 152,648,558-152,659,787 LCE2B, LCE2C
    nsv5385388copy number variation1nstd186human GRCh37 chr1: 152,648,702-152,659,620 , GRCh38.p12 chr1: 152,676,226-152,687,144 LCE2B, LCE2C
    nsv5383501copy number variation1nstd186human GRCh37 chr1: 152,648,703-152,659,620 , GRCh38.p12 chr1: 152,676,227-152,687,144 LCE2B, LCE2C
    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
    nsv5286776copy number variation1nstd204human GRCh38.p13 chr1: 152,675,978-152,687,412 , GRCh37.p13 chr1: 152,648,454-152,659,888 LCE2C, LCE2B
    nsv5207802copy number variation1nstd204human GRCh38.p13 chr1: 152,676,301-152,686,600 , GRCh37.p13 chr1: 152,648,777-152,659,076 LCE2C, LCE2B
    nsv5079612mobile element insertion1nstd203human GRCh38 chr1: 152,684,560-152,684,570 , GRCh37.p13 chr1: 152,657,036-152,657,046 LCE2B
    nsv5066007mobile element insertion1nstd203human GRCh38 chr1: 152,684,562-152,684,570 , GRCh37.p13 chr1: 152,657,038-152,657,046 LCE2B
    nsv5062211mobile element insertion1nstd203human GRCh38 chr1: 152,684,555-152,684,570 , GRCh37.p13 chr1: 152,657,031-152,657,046 LCE2B
    nsv4903879copy number variation1nstd200human GRCh38 chr1: 152,676,226-152,687,145 , GRCh37.p13 chr1: 152,648,702-152,659,621 LCE2C, LCE2B
    nsv4903878copy number variation1nstd200human GRCh38 chr1: 152,674,473-152,685,568 , GRCh37.p13 chr1: 152,646,949-152,658,044 LCE2B, LCE2C
    nsv4903877copy number variation1nstd200human GRCh38 chr1: 152,664,829-152,687,770 , GRCh37.p13 chr1: 152,637,305-152,660,246 LCE2C, LCE2D, 1 more genes
    nsv4897424copy number variation1nstd200human GRCh38 chr1: 152,664,371-152,687,075 , GRCh37.p13 chr1: 152,636,847-152,659,551 LCE2D, LCE2B, 1 more genes
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