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Items: 1 to 20 of 239

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5976694inversion1nstd209human GRCh38 chr5: 179,854,164-180,408,925 , GRCh37.p13 chr5: 179,281,164-179,835,925 MAPK9, GFPT2, 11 more genes
    nsv5954841insertion1nstd209human GRCh38 chr5: 180,246,849-180,246,849 , GRCh37.p13 chr5: 179,673,849-179,673,849 MAPK9
    nsv5887834copy number variation1nstd209human GRCh38 chr5: 180,268,557-180,268,868 , GRCh37.p13 chr5: 179,695,557-179,695,868 MAPK9
    nsv5887728copy number variation1nstd209human GRCh38 chr5: 180,286,145-180,286,722 , GRCh37.p13 chr5: 179,713,145-179,713,722 MAPK9
    nsv5694296mobile element insertion2nstd211human GRCh38 chr5: 180,246,865-180,246,865 , GRCh37.p13 chr5: 179,673,865-179,673,865 MAPK9
    nsv5682504mobile element insertion2nstd211human GRCh38 chr5: 180,234,765-180,234,765 , GRCh37.p13 chr5: 179,661,765-179,661,765 MAPK9
    nsv5564999copy number variation1nstd207human GRCh38 chr5: 180,286,145-180,286,722 , GRCh37.p13 chr5: 179,713,145-179,713,722 MAPK9
    nsv5561640sequence alteration1nstd206human GRCh38 chr5: 179,554,688-180,310,132 , GRCh37.p13 chr5: 178,981,689-179,737,132 LTC4S, MIR340, 28 more genes
    nsv5559986sequence alteration1nstd206human GRCh38 chr5: 180,285,839-180,286,435 , GRCh37.p13 chr5: 179,712,839-179,713,435 MAPK9
    nsv5471815copy number variation1nstd206human GRCh38 chr5: 180,267,769-180,268,723 , GRCh37.p13 chr5: 179,694,769-179,695,723 MAPK9
    nsv5464414copy number variation1nstd206human GRCh38 chr5: 180,286,146-180,286,723 , GRCh37.p13 chr5: 179,713,146-179,713,723 MAPK9
    nsv5455246copy number variation1nstd206human GRCh38 chr5: 180,268,557-180,268,889 , GRCh37.p13 chr5: 179,695,557-179,695,889 MAPK9
    nsv5413460mobile element insertion1nstd206human GRCh38 chr5: 180,234,765-180,234,816 , GRCh37.p13 chr5: 179,661,765-179,661,816 MAPK9
    nsv5400744mobile element insertion1nstd206human GRCh38 chr5: 180,246,865-180,246,916 , GRCh37.p13 chr5: 179,673,865-179,673,916 MAPK9
    nsv5386990copy number variation2nstd186human GRCh37 chr5: 179,713,146-179,713,723 , GRCh38.p12 chr5: 180,286,146-180,286,723 MAPK9
    nsv5322696translocation1nstd204human GRCh38.p13 chr5: 180,286,146-180,286,146 , GRCh38.p13 chr5: 180,286,723-180,286,723 , GRCh37.p13 chr5: 179,713,723-179,713,723 , GRCh37.p13 chr5: 179,713,146-179,713,146 MAPK9
    nsv5301596copy number variation1nstd204human GRCh38.p13 chr5: 179,616,292-180,442,361 , GRCh37.p13 chr5: 179,043,293-179,869,361 MIR1229, MAPK9, 25 more genes
    nsv5229540copy number variation1nstd204human GRCh38.p13 chr5: 179,907,701-180,437,500 , GRCh37.p13 chr5: 179,334,701-179,864,500 RPS15AP18, LOC646058, 9 more genes
    nsv5089824mobile element insertion1nstd203human GRCh38 chr5: 180,246,849-180,246,865 , GRCh37.p13 chr5: 179,673,849-179,673,865 MAPK9
    nsv5083998mobile element insertion1nstd203human GRCh38 chr5: 180,266,751-180,266,762 , GRCh37.p13 chr5: 179,693,751-179,693,762 MAPK9
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