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Items: 1 to 20 of 329

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5926416copy number variation1nstd209human GRCh38 chr10: 14,981,142-14,993,328 , GRCh37.p13 chr10: 15,023,141-15,035,327 OR7E110P, MEIG1
    nsv5922896copy number variation1nstd209human GRCh38 chr10: 14,985,156-14,985,216 , GRCh37.p13 chr10: 15,027,155-15,027,215 MEIG1, OR7E110P
    nsv5917758copy number variation1nstd209human GRCh38 chr10: 14,984,161-14,984,238 , GRCh37.p13 chr10: 15,026,160-15,026,237 MEIG1
    nsv5913847copy number variation1nstd209human GRCh38 chr10: 14,987,301-15,008,677 , GRCh37.p13 chr10: 15,029,300-15,050,676 OR7E115P, OR7E110P, 2 more genes
    nsv5913105copy number variation1nstd209human GRCh38 chr10: 14,987,586-15,008,841 , GRCh37.p13 chr10: 15,029,585-15,050,840 OR7E115P, OR7E110P, 2 more genes
    nsv5909983copy number variation1nstd209human GRCh38 chr10: 14,982,842-14,994,985 , GRCh37.p13 chr10: 15,024,841-15,036,984 OR7E110P, MEIG1
    nsv5866373copy number variation1nstd209human GRCh38 chr10: 14,954,048-14,956,047 , GRCh37.p13 chr10: 14,996,047-14,998,046 DCLRE1C, MEIG1
    nsv5858095copy number variation1nstd209human GRCh38 chr10: 14,945,634-14,957,297 , GRCh37.p13 chr10: 14,987,633-14,999,296 MEIG1, DCLRE1C
    nsv5855807copy number variation1nstd209human GRCh38 chr10: 14,966,485-15,021,450 , GRCh37.p13 chr10: 15,008,484-15,063,449 OR7E115P, OR7E110P, 4 more genes
    nsv5847606copy number variation2nstd209human GRCh38 chr10: 14,987,337-15,008,793 , GRCh37.p13 chr10: 15,029,336-15,050,792 OR7E110P, MEIG1, 2 more genes
    nsv5585405copy number variation1nstd207human GRCh38 chr10: 14,933,455-15,015,970 , GRCh37.p13 chr10: 14,975,454-15,057,969 DCLRE1C, OR7E115P, 5 more genes
    nsv5544781insertion1nstd206human GRCh38 chr10: 14,974,924-14,975,060 , GRCh37.p13 chr10: 15,016,923-15,017,059 MEIG1
    nsv5491175copy number variation1nstd206human GRCh38 chr10: 14,951,998-15,023,291 , GRCh37.p13 chr10: 14,993,997-15,065,290 DCLRE1C, OR7E115P, 5 more genes
    nsv5487491copy number variation1nstd206human GRCh38 chr10: 14,977,600-14,979,750 , GRCh37.p13 chr10: 15,019,599-15,021,749 MEIG1
    nsv5483571copy number variation1nstd206human GRCh38 chr10: 14,985,156-14,985,225 , GRCh37.p13 chr10: 15,027,155-15,027,224 MEIG1, OR7E110P
    nsv5483255copy number variation1nstd206human GRCh38 chr10: 14,950,103-15,005,437 , GRCh37.p13 chr10: 14,992,102-15,047,436 DCLRE1C, OR7E110P, 2 more genes
    nsv5381768copy number variation1nstd102humanPathogenic GRCh37 chr10: 9,137,489-17,227,168 , GRCh38.p12 chr10: 9,095,526-17,185,169 PROSER2, C1QL3, 110 more genes
    nsv5344015translocation1nstd200human GRCh37 chr10: 15,016,546-15,016,546 , GRCh37 chr10: 15,024,607-15,024,607 , GRCh38.p12 chr10: 14,974,547-14,974,547 , GRCh38.p12 chr10: 14,982,608-14,982,608 MEIG1
    nsv5301291copy number variation1nstd204human GRCh38.p13 chr10: 14,968,202-14,973,540 , GRCh37.p13 chr10: 15,010,201-15,015,539 MEIG1
    nsv5248476copy number variation1nstd204human GRCh38.p13 chr10: 14,968,585-14,973,568 , GRCh37.p13 chr10: 15,010,584-15,015,567 MEIG1
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