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Items: 1 to 20 of 338

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5965599insertion1nstd209human GRCh38 chr3: 194,654,083-194,654,083 , GRCh37.p13 chr3: 194,374,812-194,374,812 LSG1
    nsv5962536insertion1nstd209human GRCh38 chr3: 194,667,943-194,667,943 , GRCh37.p13 chr3: 194,388,672-194,388,672 LSG1
    nsv5948665insertion1nstd209human GRCh38 chr3: 194,644,386-194,644,386 , GRCh37.p13 chr3: 194,365,115-194,365,115 LSG1
    nsv5892017copy number variation1nstd209human GRCh38 chr3: 194,663,356-194,663,747 , GRCh37.p13 chr3: 194,384,085-194,384,476 LSG1
    nsv5685914mobile element insertion2nstd211human GRCh38 chr3: 194,654,098-194,654,098 , GRCh37.p13 chr3: 194,374,827-194,374,827 LSG1
    nsv5683054mobile element insertion2nstd211human GRCh38 chr3: 194,641,883-194,641,883 , GRCh37.p13 chr3: 194,362,612-194,362,612 LSG1
    nsv5622905insertion1nstd207human GRCh38 chr3: 194,645,593-194,645,593 , GRCh37.p13 chr3: 194,366,322-194,366,322 LSG1
    nsv5622219insertion1nstd207human GRCh38 chr3: 194,654,083-194,654,083 , GRCh37.p13 chr3: 194,374,812-194,374,812 LSG1
    nsv5613348insertion1nstd207human GRCh38 chr3: 194,641,865-194,641,865 , GRCh37.p13 chr3: 194,362,594-194,362,594 LSG1
    nsv5576232copy number variation1nstd207human GRCh38 chr3: 194,645,519-194,645,574 , GRCh37.p13 chr3: 194,366,248-194,366,303 LSG1
    nsv5568876copy number variation1nstd207human GRCh38 chr3: 194,663,356-194,663,747 , GRCh37.p13 chr3: 194,384,085-194,384,476 LSG1
    nsv5559488sequence alteration1nstd206human GRCh37.p13 chr3: 194,362,410-194,675,824 , GRCh38 chr3: 194,641,681-194,955,095 , LSG1, 6 more genes
    nsv5553393insertion1nstd206human GRCh38 chr3: 194,641,883-194,641,916 , GRCh37.p13 chr3: 194,362,612-194,362,645 LSG1
    nsv5453639copy number variation1nstd206human GRCh38 chr3: 163,047,000-198,226,000 , GRCh37.p13 chr3: 162,764,788-197,952,871 , MIR922, 587 more genes
    nsv5449508copy number variation1nstd206human GRCh38 chr3: 194,433,000-194,791,574 , GRCh37.p13 chr3: 194,153,729-194,512,303 RNU6-1101P, FAM151AP1, 11 more genes
    nsv5396759mobile element insertion1nstd206human GRCh38 chr3: 194,654,098-194,654,133 , GRCh37.p13 chr3: 194,374,827-194,374,862 LSG1
    nsv5385818copy number variation1nstd186human GRCh37 chr3: 194,384,122-194,384,471 , GRCh38.p12 chr3: 194,663,393-194,663,742 LSG1
    nsv5385796copy number variation1nstd186human GRCh37 chr3: 194,384,175-194,384,452 , GRCh38.p12 chr3: 194,663,446-194,663,723 LSG1
    nsv5352379translocation1nstd200human GRCh38 chr3: 194,643,712-194,643,712 , GRCh38 chr3: 194,643,770-194,643,770 , GRCh37.p13 chr3: 194,364,441-194,364,441 , GRCh37.p13 chr3: 194,364,499-194,364,499 LSG1
    nsv5303013copy number variation1nstd204human GRCh38.p13 chr3: 194,663,091-194,664,003 , GRCh37.p13 chr3: 194,383,820-194,384,732 LSG1
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