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Items: 1 to 20 of 191

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5871835copy number variation1nstd209human GRCh38 chr1: 150,718,959-150,719,292 , GRCh37.p13 chr1: 150,691,435-150,691,768 HORMAD1
    nsv5716084mobile element insertion1nstd211human GRCh38 chr1: 150,713,685-150,713,685 , GRCh37.p13 chr1: 150,686,161-150,686,161 HORMAD1
    nsv5687225mobile element insertion1nstd211human GRCh38 chr1: 150,711,810-150,711,810 , GRCh37.p13 chr1: 150,684,286-150,684,286 HORMAD1
    nsv5569046copy number variation1nstd207human GRCh38 chr1: 150,718,959-150,719,292 , GRCh37.p13 chr1: 150,691,435-150,691,768 HORMAD1
    nsv5563405mobile element insertion1nstd206human GRCh38 chr1: 150,713,685-150,713,688 , GRCh37.p13 chr1: 150,686,161-150,686,164 HORMAD1
    nsv5423219copy number variation1nstd206human GRCh38 chr1: 150,718,975-150,719,293 , GRCh37.p13 chr1: 150,691,451-150,691,769 HORMAD1
    nsv5416307copy number variation1nstd206human GRCh38 chr1: 150,721,371-150,722,424 , GRCh37.p13 chr1: 150,693,847-150,694,900 HORMAD1
    nsv5393965mobile element insertion1nstd206human GRCh38 chr1: 150,711,810-150,711,861 , GRCh37.p13 chr1: 150,684,286-150,684,337 HORMAD1
    nsv5382098mobile element deletion2nstd186human GRCh37 chr1: 150,691,451-150,691,769 , GRCh38.p12 chr1: 150,718,975-150,719,293 HORMAD1
    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
    nsv5297347copy number variation1nstd204human GRCh37.p13 chr1: 150,671,970-150,675,501 , GRCh38.p13 chr1: 150,699,494-150,703,025 RNU6-1042P, HORMAD1
    nsv5217007copy number variation1nstd204human GRCh38.p13 chr1: 150,699,554-150,702,807 , GRCh37.p13 chr1: 150,672,030-150,675,283 HORMAD1, RNU6-1042P
    nsv5202595mobile element deletion1nstd204human GRCh38.p13 chr1: 150,718,975-150,719,293 , GRCh37.p13 chr1: 150,691,451-150,691,769 HORMAD1
    nsv4903842copy number variation1nstd200human GRCh38 chr1: 150,406,738-150,700,622 , GRCh37.p13 chr1: 150,440,214-150,673,098 ADAMTSL4, ADAMTSL4-AS1, 16 more genes
    nsv4897341copy number variation1nstd200human GRCh38 chr1: 150,721,399-150,736,011 , GRCh37.p13 chr1: 150,693,875-150,708,487 CTSS, HORMAD1
    nsv4897340copy number variation1nstd200human GRCh38 chr1: 150,699,524-150,702,996 , GRCh37.p13 chr1: 150,672,000-150,675,472 HORMAD1, RNU6-1042P
    nsv4886871mobile element deletion1nstd200human GRCh38 chr1: 150,718,975-150,719,293 , GRCh37.p13 chr1: 150,691,451-150,691,769 HORMAD1
    nsv4773982mobile element deletion1nstd200human GRCh37 chr1: 150,691,451-150,691,769 , GRCh38.p12 chr1: 150,718,975-150,719,293 HORMAD1
    nsv4773981copy number variation1nstd200human GRCh37 chr1: 150,672,000-150,675,472 , GRCh38.p12 chr1: 150,699,524-150,702,996 RNU6-1042P, HORMAD1
    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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