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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5693490mobile element insertion1nstd211human GRCh38 chr1: 170,173,949-170,173,949 , GRCh37.p13 chr1: 170,143,090-170,143,090 LINC01681
    nsv5686470mobile element insertion1nstd211human GRCh38 chr1: 170,211,998-170,211,998 , GRCh37.p13 chr1: 170,181,139-170,181,139 LINC01681
    nsv5679437mobile element insertion1nstd211human GRCh38 chr1: 170,195,711-170,195,711 , GRCh37.p13 chr1: 170,164,852-170,164,852 LINC01681
    nsv5432353copy number variation1nstd206human GRCh38 chr1: 170,174,192-170,174,339 , GRCh37.p13 chr1: 170,143,333-170,143,480 LINC01681
    nsv5430361copy number variation1nstd206human GRCh38 chr1: 170,222,109-170,222,289 , GRCh37.p13 chr1: 170,191,250-170,191,430 LINC01681
    nsv5402456mobile element insertion1nstd206human GRCh38 chr1: 170,173,949-170,174,000 , GRCh37.p13 chr1: 170,143,090-170,143,141 LINC01681
    nsv5398390mobile element insertion1nstd206human GRCh38 chr1: 170,211,998-170,212,049 , GRCh37.p13 chr1: 170,181,139-170,181,190 LINC01681
    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
    nsv5078787mobile element insertion1nstd203human GRCh38 chr1: 170,211,981-170,211,998 , GRCh37.p13 chr1: 170,181,122-170,181,139 LINC01681
    nsv5075037mobile element insertion1nstd203human GRCh38 chr1: 170,211,995-170,211,995 , GRCh37.p13 chr1: 170,181,136-170,181,136 LINC01681
    nsv5071790mobile element insertion1nstd203human GRCh38 chr1: 170,173,934-170,173,949 , GRCh37.p13 chr1: 170,143,075-170,143,090 LINC01681
    nsv5062552mobile element insertion1nstd203human GRCh38 chr1: 170,211,994-170,211,994 , GRCh37.p13 chr1: 170,181,135-170,181,135 LINC01681
    nsv4904017copy number variation1nstd200human GRCh38 chr1: 170,231,621-170,235,154 , GRCh37.p13 chr1: 170,200,762-170,204,295 LINC01681
    nsv4897985copy number variation1nstd200human GRCh38 chr1: 170,230,229-170,230,318 , GRCh37.p13 chr1: 170,199,370-170,199,459 LINC01681
    nsv4897984copy number variation1nstd200human GRCh38 chr1: 170,226,358-170,230,209 , GRCh37.p13 chr1: 170,195,499-170,199,350 LINC01681
    nsv4897983copy number variation1nstd200human GRCh38 chr1: 170,175,070-170,176,395 , GRCh37.p13 chr1: 170,144,211-170,145,536 LINC01681
    nsv4784642copy number variation1nstd200human GRCh37 chr1: 170,195,499-170,199,350 , GRCh38.p12 chr1: 170,226,358-170,230,209 LINC01681
    nsv4767860inversion1nstd199human GRCh37 chr1: 17,051,740-234,912,187 , GRCh38.p12 chr1: 16,725,245-234,776,440 , ABCA4, 4269 more genes
    nsv4751400inversion1nstd199human GRCh37 chr1: 17,125,657-234,919,132 , GRCh38.p12 chr1: 16,799,162-234,783,385 , ABCA4, 4264 more genes
    nsv4674768copy number variation1nstd102humanPathogenic GRCh37 chr1: 167,430,471-174,635,618 , GRCh38.p12 chr1: 167,461,234-174,666,480 ATP1B1, RNU6-693P, 156 more genes
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