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Items: 1 to 20 of 90

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3900963copy number variation1nstd102humanLikely benign GRCh37 chr16: 28,486,693-28,578,470 , GRCh38.p12 chr16: 28,475,372-28,567,149 NUPR1, SGF29, 3 more genes
    nsv3878608copy number variation1nstd102humanPathogenic GRCh37 chr16: 28,498,777-28,607,251 , GRCh38 chr16: 28,487,456-28,595,930 NUPR1, CLN3, 4 more genes
    nsv3905855copy number variation1nstd102humanPathogenic GRCh37 chr16: 21,596,299-30,399,167 , GRCh38.p12 chr16: 21,584,978-30,387,846 NUPR1, LOC107984874, 217 more genes
    nsv6290289copy number variation1nstd102humanPathogenic GRCh37 chr16: 21,594,997-29,625,302 , GRCh38.p12 chr16: 21,583,676-29,613,981 NUPR1, LOC105371149, 166 more genes
    nsv3891271copy number variation1nstd102humanPathogenic GRCh37 chr16: 21,379,628-29,379,768 , GRCh38.p12 chr16: 21,368,307-29,368,447 NUPR1, LOC101927814, 159 more genes
    nsv6289847copy number variation1nstd102humanPathogenic GRCh37 chr16: 21,530,207-29,332,245 , GRCh38.p12 chr16: 21,518,886-29,320,924 NUPR1, GAPDHP35, 154 more genes
    nsv7137115copy number variation1nstd102humanPathogenic GRCh37 chr16: 21,467,726-29,044,717 , GRCh38.p12 chr16: 21,456,405-29,033,396 NUPR1, OTOAP1, 148 more genes
    nsv3913702copy number variation1nstd102humanPathogenic NCBI36 chr16: 28,311,654-30,239,515 , GRCh37 chr16: 28,404,153-30,332,014 , GRCh38 chr16: 28,392,832-30,320,693 NUPR1, SPN, 94 more genes
    nsv6637500copy number variation1nstd102humanPathogenic GRCh37 chr16: 28,466,731-30,321,320 , GRCh38.p12 chr16: 28,455,410-30,309,999 NUPR1, CA5AP1, 92 more genes
    nsv3915125copy number variation1nstd102humanPathogenic GRCh38 chr16: 28,456,967-30,295,107 , GRCh37 chr16: 28,468,288-30,306,428 , NCBI36 chr16: 28,375,789-30,213,929 NUPR1, SULT1A1, 92 more genes
    nsv3924589copy number variation1nstd102humanPathogenic NCBI36 chr16: 28,310,915-30,104,908 , GRCh37.p13 chr16: 28,403,414-30,197,407 , GRCh38.p12 chr16: 28,392,093-30,186,086 NUPR1, MIR4517, 86 more genes
    nsv3920951copy number variation1nstd102humanPathogenic NCBI36 chr16: 28,311,654-30,104,842 , GRCh37 chr16: 28,404,153-30,197,341 , GRCh38 chr16: 28,392,832-30,186,020 NUPR1, TBX6, 86 more genes
    nsv3907632copy number variation1nstd102humanPathogenic GRCh37 chr16: 28,441,538-30,178,406 , GRCh38.p12 chr16: 28,430,217-30,167,085 NUPR1, LOC102723708, 82 more genes
    nsv4455909copy number variation1nstd102humanPathogenic GRCh37 chr16: 28,466,730-30,191,848 , GRCh38.p12 chr16: 28,455,409-30,180,527 NUPR1, BOLA2, 82 more genes
    nsv4674913copy number variation1nstd102humanPathogenic GRCh37 chr16: 28,466,730-30,178,406 , GRCh38.p12 chr16: 28,455,409-30,167,085 NUPR1, ATP2A1, 82 more genes
    nsv4455681copy number variation1nstd102humanPathogenic GRCh37 chr16: 28,466,730-30,177,916 , GRCh38.p12 chr16: 28,455,409-30,166,595 NUPR1, SMG1P2, 82 more genes
    nsv3898101copy number variation1nstd102humanPathogenic GRCh37 chr16: 28,486,693-30,197,290 , GRCh38.p12 chr16: 28,475,372-30,185,969 NUPR1, TAOK2, 83 more genes
    nsv3915205copy number variation1nstd102humanPathogenic NCBI36 chr16: 28,406,323-30,104,908 , GRCh37.p13 chr16: 28,498,822-30,197,407 , GRCh38.p12 chr16: 28,487,501-30,186,086 NUPR1, TMEM219, 83 more genes
    nsv4729918copy number variation1nstd102humanPathogenic GRCh37 chr16: 28,488,319-30,178,406 , GRCh38.p12 chr16: 28,476,998-30,167,085 NUPR1, SEZ6L2, 81 more genes
    nsv3923420copy number variation1nstd102humanPathogenic NCBI36 chr16: 28,450,605-30,102,254 , GRCh37 chr16: 28,543,104-30,194,753 , GRCh38 chr16: 28,531,783-30,183,432 NUPR1, KCTD13, 80 more genes
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