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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5943566copy number variation1nstd209human GRCh38 chr17: 60,611,164-60,612,006 , GRCh37.p13 chr17: 58,688,525-58,689,367 PPM1D
    nsv5939305copy number variation1nstd209human GRCh38 chr17: 60,645,612-60,645,673 , GRCh37.p13 chr17: 58,722,973-58,723,034 PPM1D
    nsv5938375copy number variation1nstd209human GRCh38 chr17: 60,654,257-60,654,374 , GRCh37.p13 chr17: 58,731,618-58,731,735 PPM1D
    nsv5931144copy number variation1nstd209human GRCh38 chr17: 60,645,432-60,645,669 , GRCh37.p13 chr17: 58,722,793-58,723,030 PPM1D
    nsv5868751copy number variation1nstd209human GRCh38 chr17: 60,658,070-60,660,030 , GRCh37.p13 chr17: 58,735,431-58,737,391 PPM1D
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5532268copy number variation1nstd206human GRCh38 chr17: 60,620,645-60,621,666 , GRCh37.p13 chr17: 58,698,006-58,699,027 PPM1D
    nsv5527222copy number variation1nstd206human GRCh38 chr17: 60,648,658-60,648,893 , GRCh37.p13 chr17: 58,726,019-58,726,254 PPM1D
    nsv5517031copy number variation1nstd206human GRCh38 chr17: 60,607,353-60,609,282 , GRCh37.p13 chr17: 58,684,714-58,686,643 PPM1D
    nsv5010480copy number variation1nstd200human GRCh38 chr17: 60,649,191-60,654,382 , GRCh37.p13 chr17: 58,726,552-58,731,743 PPM1D
    nsv5010479copy number variation1nstd200human GRCh38 chr17: 60,648,658-60,648,893 , GRCh37.p13 chr17: 58,726,019-58,726,254 PPM1D
    nsv4851553copy number variation1nstd200human GRCh37 chr17: 58,726,019-58,726,254 , GRCh38.p12 chr17: 60,648,658-60,648,893 PPM1D
    nsv4851552copy number variation1nstd200human GRCh37 chr17: 58,714,038-58,714,546 , GRCh38.p12 chr17: 60,636,677-60,637,185 PPM1D
    nsv4729908copy number variation1nstd102humanUncertain significance GRCh37 chr17: 58,713,087-59,030,337 , GRCh38.p12 chr17: 60,635,726-60,952,976 KRT18P61, HMGN1P28, 6 more genes
    nsv4671799copy number variation1nstd186human GRCh37 chr17: 58,740,945-58,741,004 , GRCh38.p12 chr17: 60,663,584-60,663,643 PPM1D
    nsv4632713copy number variation1nstd183human GRCh37 chr17: 58,740,945-58,741,004 , GRCh38.p12 chr17: 60,663,584-60,663,643 PPM1D
    nsv4626289copy number variation1nstd183human GRCh37 chr17: 58,740,945-58,741,285 , GRCh38.p12 chr17: 60,663,584-60,663,924 PPM1D
    nsv4554373insertion1nstd166human GRCh37.p13 chr17: 58,680,717-58,680,717 , GRCh38.p12 chr17: 60,603,356-60,603,356 PPM1D
    nsv4502389mobile element insertion1nstd166human GRCh37.p13 chr17: 58,701,685-58,701,685 , GRCh38.p12 chr17: 60,624,324-60,624,324 PPM1D
    nsv4457838copy number variation1nstd102humanUncertain significance GRCh37 chr17: 58,345,523-58,736,414 , GRCh38.p12 chr17: 60,268,162-60,659,053 LOC107984970, H3P42, 9 more genes
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