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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
    nsv6129308insertion1nstd186human GRCh37 chr19: 37,742,680-37,742,683 , GRCh38.p12 chr19: 37,251,778-37,251,781 LINC01535
    nsv5978594insertion1nstd209human GRCh38 chr19: 37,251,761-37,251,761 , GRCh37.p13 chr19: 37,742,663-37,742,663 LINC01535
    nsv5935357copy number variation1nstd209human GRCh38 chr19: 36,793,433-37,314,449 , GRCh37.p13 chr19: 37,284,335-37,805,351 ZNF875, ZNF585A, 12 more genes
    nsv5881045copy number variation2nstd209human GRCh38 chr19: 37,255,539-37,261,879 , GRCh37.p13 chr19: 37,746,441-37,752,781 LINC01535
    nsv5714035mobile element insertion1nstd211human GRCh38 chr19: 37,253,225-37,253,225 , GRCh37.p13 chr19: 37,744,127-37,744,127 LINC01535
    nsv5668400inversion1nstd207human GRCh38 chr19: 37,191,088-37,309,822 , GRCh37.p13 chr19: 37,681,990-37,800,724 ZNF585B, ZNF383, 2 more genes
    nsv5659006insertion1nstd207human GRCh38 chr19: 37,251,761-37,251,761 , GRCh37.p13 chr19: 37,742,663-37,742,663 LINC01535
    nsv5552643insertion1nstd206human GRCh38 chr19: 37,251,778-37,251,781 , GRCh37.p13 chr19: 37,742,680-37,742,683 LINC01535
    nsv5289079copy number variation1nstd204human GRCh38.p13 chr19: 37,262,601-37,263,100 , GRCh37.p13 chr19: 37,753,503-37,754,002 LINC01535
    nsv5166953mobile element insertion1nstd203human GRCh38 chr19: 37,251,698-37,251,713 , GRCh37.p13 chr19: 37,742,600-37,742,615 LINC01535
    nsv5027807copy number variation1nstd200human GRCh38 chr19: 37,254,374-37,255,601 , GRCh37.p13 chr19: 37,745,276-37,746,503 LINC01535
    nsv4755846insertion1nstd199human GRCh37 chr19: 37,742,672-37,742,672 , GRCh38.p12 chr19: 37,251,770-37,251,770 LINC01535
    nsv4724898insertion1nstd186human GRCh37 chr19: 37,742,663-37,742,663 , GRCh38.p12 chr19: 37,251,761-37,251,761 LINC01535
    nsv4626882copy number variation1nstd183human GRCh37 chr19: 37,743,191-37,749,697 , GRCh38.p12 chr19: 37,252,289-37,258,795 LINC01535
    nsv4620128copy number variation2nstd183human GRCh37 chr19: 37,756,832-37,796,253 , GRCh38.p12 chr19: 37,265,930-37,305,351 LINC01535, LOC284412
    nsv4541361insertion1nstd166human GRCh37.p13 chr19: 37,742,663-37,742,663 , GRCh38.p12 chr19: 37,251,761-37,251,761 LINC01535
    nsv4457372copy number variation1nstd102humanPathogenic GRCh37 chr19: 28,271,106-49,213,832 , GRCh38.p12 chr19: 27,780,198-48,710,575 ZNF461, LOC101927572, 735 more genes
    nsv4441795insertion1nstd175human GRCh37 chr19: 37,742,663-37,742,663 , GRCh38.p12 chr19: 37,251,761-37,251,761 LINC01535
    nsv4436633complex substitution1nstd102humanUncertain significance GRCh38.p12 chr19: 36,183,403-38,162,322 , GRCh37 chr19: 36,674,305-38,652,962 ZNF146, ZFP30, 60 more genes
    nsv4428032copy number variation1nstd174human GRCh37 chr19: 37,721,760-37,819,273 , GRCh38.p12 chr19: 37,230,858-37,328,371 LINC01535, LOC284412, 2 more genes
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