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Items: 1 to 20 of 295

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5902061copy number variation1nstd209human GRCh38 chr5: 90,282,933-90,283,324 , GRCh37.p13 chr5: 89,578,750-89,579,141 LINC01339
    nsv5724159mobile element insertion1nstd211human GRCh38 chr5: 90,161,136-90,161,136 , GRCh37.p13 chr5: 89,456,953-89,456,953 LINC01339
    nsv5690739mobile element insertion2nstd211human GRCh38 chr5: 90,286,226-90,286,226 , GRCh37.p13 chr5: 89,582,043-89,582,043 LINC01339
    nsv5556566mobile element insertion1nstd206human GRCh38 chr5: 90,161,136-90,161,186 , GRCh37.p13 chr5: 89,456,953-89,457,003 LINC01339
    nsv5471488copy number variation1nstd206human GRCh38 chr5: 90,270,931-90,271,310 , GRCh37.p13 chr5: 89,566,748-89,567,127 LINC01339
    nsv5459544copy number variation1nstd206human GRCh38 chr5: 90,277,080-90,277,223 , GRCh37.p13 chr5: 89,572,897-89,573,040 LINC01339
    nsv5405136mobile element insertion1nstd206human GRCh38 chr5: 90,286,226-90,286,277 , GRCh37.p13 chr5: 89,582,043-89,582,094 LINC01339
    nsv5368652translocation1nstd200human GRCh38 chr5: 90,267,575-90,267,575 , GRCh38 chr5: 90,267,868-90,267,868 , GRCh37.p13 chr5: 89,563,685-89,563,685 , GRCh37.p13 chr5: 89,563,392-89,563,392 LINC01339
    nsv5094249mobile element insertion1nstd203human GRCh38 chr5: 90,175,945-90,175,945 , GRCh37.p13 chr5: 89,471,762-89,471,762 LINC01339
    nsv5093598mobile element insertion1nstd203human GRCh38 chr5: 90,176,192-90,176,234 , GRCh37.p13 chr5: 89,472,009-89,472,051 LINC01339
    nsv5036421inversion1nstd200human GRCh38 chr5: 85,193,812-162,906,830 , GRCh37.p13 chr5: 84,489,630-162,333,836 , PRR16, 1116 more genes
    nsv5033775inversion1nstd200human GRCh38 chr5: 76,373,686-102,541,075 , GRCh37.p13 chr5: 75,669,511-101,876,779 , F2RL1, 331 more genes
    nsv4949006copy number variation1nstd200human GRCh38 chr5: 90,235,784-90,236,123 , GRCh37.p13 chr5: 89,531,601-89,531,940 LINC01339
    nsv4949005copy number variation1nstd200human GRCh38 chr5: 90,160,983-90,184,548 , GRCh37.p13 chr5: 89,456,800-89,480,365 LINC01339
    nsv4947130copy number variation1nstd200human GRCh38 chr5: 90,267,242-90,268,866 , GRCh37.p13 chr5: 89,563,059-89,564,683 LINC01339
    nsv4885569inversion1nstd200human GRCh37 chr5: 84,489,636-162,333,841 , GRCh38.p12 chr5: 85,193,818-162,906,835 , UBE2B, 1116 more genes
    nsv4805656copy number variation1nstd200human GRCh37 chr5: 89,531,601-89,531,940 , GRCh38.p12 chr5: 90,235,784-90,236,123 LINC01339
    nsv4805655copy number variation1nstd200human GRCh37 chr5: 89,456,800-89,480,365 , GRCh38.p12 chr5: 90,160,983-90,184,548 LINC01339
    nsv4793271copy number variation1nstd200human GRCh37 chr5: 89,563,059-89,564,683 , GRCh38.p12 chr5: 90,267,242-90,268,866 LINC01339
    nsv4793270copy number variation1nstd200human GRCh37 chr5: 89,554,027-89,554,477 , GRCh38.p12 chr5: 90,258,210-90,258,660 LINC01339
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