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Items: 1 to 20 of 283

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5693857mobile element insertion1nstd211human GRCh38 chr1: 219,146,048-219,146,048 , GRCh37.p13 chr1: 219,319,390-219,319,390 LYPLAL1-DT
    nsv5679497mobile element insertion1nstd211human GRCh38 chr1: 219,152,787-219,152,787 , GRCh37.p13 chr1: 219,326,129-219,326,129 LYPLAL1-DT
    nsv5436780copy number variation1nstd206human GRCh38 chr1: 219,133,554-219,133,612 , GRCh37.p13 chr1: 219,306,896-219,306,954 LYPLAL1-DT
    nsv5402468mobile element insertion1nstd206human GRCh38 chr1: 219,146,048-219,146,057 , GRCh37.p13 chr1: 219,319,390-219,319,399 LYPLAL1-DT
    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
    nsv5341526translocation1nstd200human GRCh37 chr1: 219,333,075-219,333,075 , GRCh37 chr1: 219,333,352-219,333,352 , GRCh38.p12 chr1: 219,160,010-219,160,010 , GRCh38.p12 chr1: 219,159,733-219,159,733 LYPLAL1-DT
    nsv5338176translocation1nstd200human GRCh37 chr1: 219,333,344-219,333,344 , GRCh37 chr1: 219,328,087-219,328,087 , GRCh38.p12 chr1: 219,154,745-219,154,745 , GRCh38.p12 chr1: 219,160,002-219,160,002 LYPLAL1-DT
    nsv5205208copy number variation1nstd204human GRCh38.p13 chr1: 219,091,501-219,095,600 , GRCh37.p13 chr1: 219,264,843-219,268,942 LYPLAL1-DT
    nsv5201613copy number variation1nstd204human GRCh38.p13 chr1: 219,135,401-219,138,600 , GRCh37.p13 chr1: 219,308,743-219,311,942 LYPLAL1-DT
    nsv5077942mobile element insertion1nstd203human GRCh38 chr1: 219,158,318-219,158,332 , GRCh37.p13 chr1: 219,331,660-219,331,674 LYPLAL1-DT
    nsv5069000mobile element insertion1nstd203human GRCh38 chr1: 219,093,030-219,093,045 , GRCh37.p13 chr1: 219,266,372-219,266,387 LYPLAL1-DT
    nsv4904360copy number variation1nstd200human GRCh38 chr1: 219,160,282-219,160,452 , GRCh37.p13 chr1: 219,333,624-219,333,794 LYPLAL1-DT
    nsv4904359copy number variation1nstd200human GRCh38 chr1: 218,996,275-219,080,666 , GRCh37.p13 chr1: 219,169,617-219,254,008 LYPLAL1-DT
    nsv4898784copy number variation1nstd200human GRCh38 chr1: 219,127,052-219,410,069 , GRCh37.p13 chr1: 219,300,394-219,583,411 LYPLAL1, RIMKLBP2, 2 more genes
    nsv4898783copy number variation1nstd200human GRCh38 chr1: 219,087,506-219,404,470 , GRCh37.p13 chr1: 219,260,848-219,577,812 LYPLAL1, RIMKLBP2, 1 more genes
    nsv4781453copy number variation1nstd200human GRCh37 chr1: 219,333,624-219,333,794 , GRCh38.p12 chr1: 219,160,282-219,160,452 LYPLAL1-DT
    nsv4774442copy number variation1nstd200human GRCh37 chr1: 219,306,896-219,306,954 , GRCh38.p12 chr1: 219,133,554-219,133,612 LYPLAL1-DT
    nsv4774441copy number variation1nstd200human GRCh37 chr1: 219,300,394-219,583,411 , GRCh38.p12 chr1: 219,127,052-219,410,069 LOC107984018, LYPLAL1-DT, 2 more genes
    nsv4774440copy number variation1nstd200human GRCh37 chr1: 219,252,234-219,262,961 , GRCh38.p12 chr1: 219,078,892-219,089,619 LYPLAL1-DT
    nsv4767860inversion1nstd199human GRCh37 chr1: 17,051,740-234,912,187 , GRCh38.p12 chr1: 16,725,245-234,776,440 , ABCA4, 4269 more genes
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