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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5958642insertion1nstd209human GRCh38 chr1: 167,250,996-167,250,996 , GRCh37.p13 chr1: 167,220,233-167,220,233 POU2F1
    nsv5882570copy number variation1nstd209human GRCh38 chr1: 167,375,782-167,375,886 , GRCh37.p13 chr1: 167,345,019-167,345,123 POU2F1
    nsv5880516copy number variation1nstd209human GRCh38 chr1: 167,324,382-167,324,444 , GRCh37.p13 chr1: 167,293,619-167,293,681 POU2F1
    nsv5878981copy number variation1nstd209human GRCh38 chr1: 167,427,843-167,428,811 , GRCh37.p13 chr1: 167,397,080-167,398,048 POU2F1, CD247
    nsv5878774copy number variation1nstd209human GRCh38 chr1: 167,320,089-167,320,144 , GRCh37.p13 chr1: 167,289,326-167,289,381 POU2F1
    nsv5871998copy number variation1nstd209human GRCh38 chr1: 167,311,811-167,312,234 , GRCh37.p13 chr1: 167,281,048-167,281,471 POU2F1
    nsv5871142copy number variation1nstd209human GRCh38 chr1: 167,328,697-167,328,757 , GRCh37.p13 chr1: 167,297,934-167,297,994 POU2F1
    nsv5693719mobile element insertion1nstd211human GRCh38 chr1: 167,233,806-167,233,806 , GRCh37.p13 chr1: 167,203,043-167,203,043 POU2F1
    nsv5691769mobile element insertion1nstd211human GRCh38 chr1: 167,288,099-167,288,099 , GRCh37.p13 chr1: 167,257,336-167,257,336 POU2F1
    nsv5676409mobile element insertion1nstd211human GRCh38 chr1: 167,327,649-167,327,649 , GRCh37.p13 chr1: 167,296,886-167,296,886 POU2F1
    nsv5576461copy number variation1nstd207human GRCh38 chr1: 167,324,382-167,324,444 , GRCh37.p13 chr1: 167,293,619-167,293,681 POU2F1
    nsv5431194copy number variation1nstd206human GRCh38 chr1: 167,320,090-167,320,145 , GRCh37.p13 chr1: 167,289,327-167,289,382 POU2F1
    nsv5424779copy number variation1nstd206human GRCh38 chr1: 167,419,510-167,419,602 , GRCh37.p13 chr1: 167,388,747-167,388,839 POU2F1
    nsv5421552copy number variation1nstd206human GRCh38 chr1: 167,328,698-167,328,758 , GRCh37.p13 chr1: 167,297,935-167,297,995 POU2F1
    nsv5419143copy number variation1nstd206human GRCh38 chr1: 167,358,927-167,364,539 , GRCh37.p13 chr1: 167,328,164-167,333,776 POU2F1
    nsv5418825copy number variation1nstd206human GRCh38 chr1: 167,359,756-167,359,852 , GRCh37.p13 chr1: 167,328,993-167,329,089 POU2F1
    nsv5404203mobile element insertion1nstd206human GRCh38 chr1: 167,233,806-167,233,857 , GRCh37.p13 chr1: 167,203,043-167,203,094 POU2F1
    nsv5402138mobile element insertion1nstd206human GRCh38 chr1: 167,288,099-167,288,150 , GRCh37.p13 chr1: 167,257,336-167,257,387 POU2F1
    nsv5394055mobile element insertion1nstd206human GRCh38 chr1: 167,327,649-167,327,700 , GRCh37.p13 chr1: 167,296,886-167,296,937 POU2F1
    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
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