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Items: 1 to 20 of 256

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5682295mobile element insertion1nstd211human GRCh38 chr1: 75,736,514-75,736,514 , GRCh37.p13 chr1: 76,202,199-76,202,199 ACADM
    nsv5431614copy number variation1nstd206human GRCh38 chr1: 75,608,610-75,913,087 , GRCh37.p13 chr1: 76,074,295-76,378,772 ACADM, DLSTP1, 7 more genes
    nsv5403229mobile element insertion1nstd206human GRCh38 chr1: 75,736,514-75,736,559 , GRCh37.p13 chr1: 76,202,199-76,202,244 ACADM
    nsv5367714translocation1nstd200human GRCh38 chr1: 75,745,611-75,745,611 , GRCh38 chr1: 75,744,540-75,744,540 , GRCh37.p13 chr1: 76,210,225-76,210,225 , GRCh37.p13 chr1: 76,211,296-76,211,296 DLSTP1, ACADM
    nsv5075726mobile element insertion1nstd203human GRCh38 chr1: 75,760,547-75,760,580 , GRCh37.p13 chr1: 76,226,232-76,226,265 ACADM
    nsv5074173mobile element insertion1nstd203human GRCh38 chr1: 75,760,546-75,760,580 , GRCh37.p13 chr1: 76,226,231-76,226,265 ACADM
    nsv5071784mobile element insertion1nstd203human GRCh38 chr1: 75,736,501-75,736,514 , GRCh37.p13 chr1: 76,202,186-76,202,199 ACADM
    nsv5068219mobile element insertion1nstd203human GRCh38 chr1: 75,760,264-75,760,283 , GRCh37.p13 chr1: 76,225,949-76,225,968 ACADM
    nsv5061107mobile element insertion1nstd203human GRCh38 chr1: 75,736,504-75,736,514 , GRCh37.p13 chr1: 76,202,189-76,202,199 ACADM
    nsv5060935mobile element insertion1nstd203human GRCh38 chr1: 75,760,544-75,760,544 , GRCh37.p13 chr1: 76,226,229-76,226,229 ACADM
    nsv5060290mobile element insertion1nstd203human GRCh38 chr1: 75,753,814-75,753,814 , GRCh37.p13 chr1: 76,219,499-76,219,499 ACADM
    nsv4896427copy number variation1nstd200human GRCh38 chr1: 75,751,425-75,754,421 , GRCh37.p13 chr1: 76,217,110-76,220,106 ACADM
    nsv4896426copy number variation1nstd200human GRCh38 chr1: 75,727,236-75,740,685 , GRCh37.p13 chr1: 76,192,921-76,206,370 ACADM, DLSTP1
    nsv4896425copy number variation1nstd200human GRCh38 chr1: 75,719,012-75,725,660 , GRCh37.p13 chr1: 76,184,697-76,191,345 SLC44A5, ACADM
    nsv4888344inversion1nstd200human GRCh37 chr1: 51,769,169-94,478,994 , GRCh38.p12 chr1: 51,303,497-94,013,438 , ST13P20, 664 more genes
    nsv4783815copy number variation1nstd200human GRCh37 chr1: 76,184,697-76,191,345 , GRCh38.p12 chr1: 75,719,012-75,725,660 SLC44A5, ACADM
    nsv4767860inversion1nstd199human GRCh37 chr1: 17,051,740-234,912,187 , GRCh38.p12 chr1: 16,725,245-234,776,440 , ABCA4, 4269 more genes
    nsv4761183inversion1nstd199human GRCh37 chr1: 16,884,570-145,374,569 , GRCh38.p12 chr1: 16,558,075-149,528,945 , ABCA4, 2341 more genes
    nsv4751400inversion1nstd199human GRCh37 chr1: 17,125,657-234,919,132 , GRCh38.p12 chr1: 16,799,162-234,783,385 , ABCA4, 4264 more genes
    nsv4683435copy number variation1nstd102humanPathogenic GRCh37 chr1: 76,190,463-76,190,512 , GRCh38.p12 chr1: 75,724,778-75,724,827 ACADM
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