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Items: 1 to 20 of 204

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5718120mobile element insertion1nstd211human GRCh38 chr5: 157,498,816-157,498,816 , GRCh37.p13 chr5: 156,925,824-156,925,824 ADAM19
    nsv5691384mobile element insertion1nstd211human GRCh38 chr5: 157,490,513-157,490,513 , GRCh37.p13 chr5: 156,917,521-156,917,521 ADAM19
    nsv5686196mobile element insertion1nstd211human GRCh38 chr5: 157,547,931-157,547,931 , GRCh37.p13 chr5: 156,974,939-156,974,939 ADAM19
    nsv5677050mobile element insertion1nstd211human GRCh38 chr5: 157,490,504-157,490,504 , GRCh37.p13 chr5: 156,917,512-156,917,512 ADAM19
    nsv5561529mobile element insertion1nstd206human GRCh38 chr5: 157,498,816-157,498,867 , GRCh37.p13 chr5: 156,925,824-156,925,875 ADAM19
    nsv5558591sequence alteration1nstd206human GRCh38 chr5: 157,566,094-157,566,127 , GRCh37.p13 chr5: 156,993,102-156,993,135 ADAM19
    nsv5547696insertion1nstd206human GRCh38 chr5: 157,566,094-157,566,094 , GRCh37.p13 chr5: 156,993,102-156,993,102 ADAM19
    nsv5466261copy number variation1nstd206human GRCh38 chr5: 157,548,967-157,551,176 , GRCh37.p13 chr5: 156,975,975-156,978,184 ADAM19
    nsv5461315copy number variation1nstd206human GRCh38 chr5: 157,563,138-157,563,205 , GRCh37.p13 chr5: 156,990,146-156,990,213 ADAM19
    nsv5408486mobile element insertion1nstd206human GRCh38 chr5: 157,547,931-157,547,982 , GRCh37.p13 chr5: 156,974,939-156,974,990 ADAM19
    nsv5408326mobile element insertion1nstd206human GRCh38 chr5: 157,490,513-157,490,564 , GRCh37.p13 chr5: 156,917,521-156,917,572 ADAM19
    nsv5313152copy number variation1nstd204human GRCh38.p13 chr5: 157,479,170-157,479,828 , GRCh37.p13 chr5: 156,906,178-156,906,836 ADAM19
    nsv5095005mobile element insertion1nstd203human GRCh38 chr5: 157,569,564-157,569,579 , GRCh37.p13 chr5: 156,996,572-156,996,587 ADAM19
    nsv5081408mobile element insertion1nstd203human GRCh38 chr5: 157,490,504-157,490,513 , GRCh37.p13 chr5: 156,917,512-156,917,521 ADAM19
    nsv5036421inversion1nstd200human GRCh38 chr5: 85,193,812-162,906,830 , GRCh37.p13 chr5: 84,489,630-162,333,836 , PRR16, 1116 more genes
    nsv4939430copy number variation1nstd200human GRCh38 chr5: 157,556,603-157,556,681 , GRCh37.p13 chr5: 156,983,611-156,983,689 ADAM19
    nsv4939429copy number variation1nstd200human GRCh38 chr5: 157,527,646-157,530,751 , GRCh37.p13 chr5: 156,954,654-156,957,759 ADAM19
    nsv4885569inversion1nstd200human GRCh37 chr5: 84,489,636-162,333,841 , GRCh38.p12 chr5: 85,193,818-162,906,835 , UBE2B, 1116 more genes
    nsv4815143copy number variation1nstd200human GRCh37 chr5: 156,983,611-156,983,689 , GRCh38.p12 chr5: 157,556,603-157,556,681 ADAM19
    nsv4674945copy number variation1nstd102humanPathogenic GRCh37 chr5: 156,347,980-169,959,880 , GRCh38.p12 chr5: 156,920,969-170,532,876 LINC02227, LINC01932, 146 more genes
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