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Items: 1 to 20 of 306

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5957722insertion1nstd209human GRCh38 chr1: 179,783,725-179,783,725 , GRCh37.p13 chr1: 179,752,860-179,752,860 FAM163A
    nsv5878920copy number variation1nstd209human GRCh38 chr1: 179,733,762-179,754,845 , GRCh37.p13 chr1: 179,702,897-179,723,980 FAM163A
    nsv5828760copy number variation1nstd209human GRCh38 chr1: 179,741,615-179,743,874 , GRCh37.p13 chr1: 179,710,750-179,713,009 FAM163A
    nsv5828434copy number variation1nstd209human GRCh38 chr1: 179,733,788-179,748,632 , GRCh37.p13 chr1: 179,702,923-179,717,767 FAM163A
    nsv5685257mobile element insertion2nstd211human GRCh38 chr1: 179,801,260-179,801,260 , GRCh37.p13 chr1: 179,770,395-179,770,395 FAM163A
    nsv5683004mobile element insertion2nstd211human GRCh38 chr1: 179,727,960-179,727,960 , GRCh37.p13 chr1: 179,697,095-179,697,095 FAM163A, LOC105371635
    nsv5621094insertion1nstd207human GRCh38 chr1: 179,727,946-179,727,946 , GRCh37.p13 chr1: 179,697,081-179,697,081 FAM163A, LOC105371635
    nsv5618601insertion1nstd207human GRCh38 chr1: 179,783,732-179,783,732 , GRCh37.p13 chr1: 179,752,867-179,752,867 FAM163A
    nsv5547288insertion1nstd206human GRCh38 chr1: 179,727,960-179,728,011 , GRCh37.p13 chr1: 179,697,095-179,697,146 LOC105371635, FAM163A
    nsv5543666insertion1nstd206human GRCh38 chr1: 179,783,724-179,783,744 , GRCh37.p13 chr1: 179,752,859-179,752,879 FAM163A
    nsv5427806copy number variation1nstd206human GRCh38 chr1: 179,716,874-179,766,081 , GRCh37.p13 chr1: 179,686,009-179,735,216 LOC105371635, FAM163A
    nsv5400786mobile element insertion1nstd206human GRCh38 chr1: 179,801,260-179,801,311 , GRCh37.p13 chr1: 179,770,395-179,770,446 FAM163A
    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
    nsv5347340translocation1nstd200human GRCh38 chr1: 179,811,492-179,811,492 , GRCh38 chr1: 179,811,665-179,811,665 , GRCh37.p13 chr1: 179,780,627-179,780,627 , GRCh37.p13 chr1: 179,780,800-179,780,800 FAM163A
    nsv5286105copy number variation1nstd204human GRCh38.p13 chr1: 179,742,795-179,747,687 , GRCh37.p13 chr1: 179,711,930-179,716,822 FAM163A
    nsv5206809copy number variation1nstd204human GRCh38.p13 chr1: 179,742,801-179,747,000 , GRCh37.p13 chr1: 179,711,936-179,716,135 FAM163A
    nsv5200613copy number variation1nstd204human GRCh38.p13 chr1: 179,742,815-179,747,712 , GRCh37.p13 chr1: 179,711,950-179,716,847 FAM163A
    nsv5070607mobile element insertion1nstd203human GRCh38 chr1: 179,727,946-179,727,960 , GRCh37.p13 chr1: 179,697,081-179,697,095 FAM163A, LOC105371635
    nsv5065292mobile element insertion1nstd203human GRCh38 chr1: 179,800,279-179,800,293 , GRCh37.p13 chr1: 179,769,414-179,769,428 FAM163A
    nsv5063114mobile element insertion1nstd203human GRCh38 chr1: 179,801,244-179,801,260 , GRCh37.p13 chr1: 179,770,379-179,770,395 FAM163A
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