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Items: 1 to 20 of 214

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5946925copy number variation1nstd209human GRCh38 chr16: 89,958,215-89,958,266 , GRCh37.p13 chr16: 90,024,623-90,024,674 DEF8
    nsv5936809copy number variation1nstd209human GRCh38 chr16: 89,946,789-89,946,840 , GRCh37.p13 chr16: 90,013,197-90,013,248 DEF8
    nsv5936249copy number variation1nstd209human GRCh38 chr16: 89,946,739-89,946,790 , GRCh37.p13 chr16: 90,013,147-90,013,198 DEF8
    nsv5870362copy number variation1nstd209human GRCh38 chr16: 89,954,264-90,002,802 , GRCh37.p13 chr16: 90,020,672-90,069,210 DEF8, AFG3L1P, 1 more genes
    nsv5870181copy number variation2nstd209human GRCh38 chr16: 89,956,550-89,958,149 , GRCh37.p13 chr16: 90,022,958-90,024,557 DEF8
    nsv5662580insertion1nstd207human GRCh38 chr16: 89,949,015-89,949,015 , GRCh37.p13 chr16: 90,015,423-90,015,423 DEF8
    nsv5654959insertion1nstd207human GRCh38 chr16: 89,946,789-89,946,789 , GRCh37.p13 chr16: 90,013,197-90,013,197 DEF8
    nsv5594105copy number variation1nstd207human GRCh38 chr16: 89,948,824-89,948,973 , GRCh37.p13 chr16: 90,015,232-90,015,381 DEF8
    nsv5587956copy number variation1nstd207human GRCh38 chr16: 89,949,001-89,949,105 , GRCh37.p13 chr16: 90,015,409-90,015,513 DEF8
    nsv5560018sequence alteration1nstd206human GRCh38 chr16: 89,926,006-90,098,466 , GRCh37.p13 chr16: 89,992,414-90,164,874 GAS8-AS1, DEF8, 9 more genes
    nsv5527912copy number variation1nstd206human GRCh38 chr16: 89,951,533-89,952,132 , GRCh37.p13 chr16: 90,017,941-90,018,540 SNORA119, DEF8
    nsv4851114copy number variation1nstd200human GRCh37 chr16: 90,028,846-90,029,300 , GRCh38.p12 chr16: 89,962,438-89,962,892 DEF8
    nsv4733624copy number variation1nstd199human GRCh37 chr16: 90,015,239-90,015,298 , GRCh38.p12 chr16: 89,948,831-89,948,890 DEF8
    nsv4729945copy number variation1nstd102humanUncertain significance GRCh37 chr16: 88,222,732-90,155,062 , GRCh38.p12 chr16: 88,189,126-90,088,654 SNORD68, LOC105371412, 75 more genes
    nsv4729883copy number variation1nstd102humanUncertain significance GRCh37 chr16: 89,499,489-90,125,146 , GRCh38.p12 chr16: 89,433,081-90,058,738 DBNDD1, RNU6-430P, 32 more genes
    nsv4729842copy number variation1nstd102humanUncertain significance GRCh37 chr16: 89,156,662-90,023,446 , GRCh38.p12 chr16: 89,090,254-89,957,038 ZNF778, SPATA2L, 33 more genes
    nsv4685754copy number variation1nstd102humannot provided GRCh37 chr16: 61,524,229-90,155,062 , GRCh38.p12 chr16: 61,490,325-90,088,654 LOC100422319, MLYCD, 547 more genes
    nsv4630715copy number variation1nstd183human GRCh37 chr16: 90,015,161-90,015,840 , GRCh38.p12 chr16: 89,948,753-89,949,432 DEF8
    nsv4628649copy number variation1nstd183human GRCh37 chr16: 90,015,161-90,015,235 , GRCh38.p12 chr16: 89,948,753-89,948,827 DEF8
    nsv4626262copy number variation2nstd183human GRCh37 chr16: 89,933,271-90,104,099 , GRCh38.p12 chr16: 89,866,863-90,037,691 GAS8, CENPBD1P, 10 more genes
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