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Items: 1 to 20 of 548

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112769copy number variation1nstd102humanPathogenic GRCh37 chr15: 30,935,243-32,445,105 , GRCh38.p12 chr15: 30,643,040-32,152,904 LOC101930434, MTMR10, 21 more genes
    nsv5973188inversion1nstd209human GRCh38 chr15: 30,730,483-31,672,938 , GRCh37.p13 chr15: 31,022,686-31,965,141 , TRPM1, 21 more genes
    nsv5710877mobile element insertion1nstd211human GRCh38 chr15: 31,395,755-31,395,755 , GRCh37.p13 chr15: 31,687,958-31,687,958 KLF13, LOC105370939
    nsv5672663copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr15: 31,196,867-32,404,120 , GRCh38.p12 chr15|NT_187660.1: 3,190,396-4,397,060 , GRCh38.p12 chr15: 30,904,664-32,111,919 , GRCh38.p12 chr15|NW_011332701.1: 3,077,944-4,284,608 MTMR10, CHRNA7, 16 more genes
    nsv5669724inversion1nstd207human GRCh38 chr15: 30,618,104-32,153,204 , GRCh37.p13 chr15: 30,910,307-32,445,405 , CHRNA7, 26 more genes
    nsv5653465insertion1nstd207human GRCh38 chr15: 31,395,741-31,395,741 , GRCh37.p13 chr15: 31,687,944-31,687,944 KLF13, LOC105370939
    nsv5429217mobile element insertion1nstd206human GRCh38 chr15: 31,395,755-31,395,806 , GRCh37.p13 chr15: 31,687,958-31,688,009 KLF13, LOC105370939
    nsv5275302copy number variation1nstd204human GRCh38.p13 chr15: 31,379,381-31,400,706 , GRCh37.p13 chr15: 31,671,584-31,692,909 LOC105370939, KLF13
    nsv5268430copy number variation1nstd204human GRCh38.p13 chr15: 31,355,744-31,392,578 , GRCh37.p13 chr15: 31,647,947-31,684,781 KLF13, LOC105370939
    nsv5200372copy number variation2nstd102humanPathogenic GRCh37 chr15: 30,943,903-32,510,863 , GRCh38.p12 chr15: 30,651,700-32,218,662 TRPM1, LOC102724078, 21 more genes
    nsv5200367copy number variation1nstd102humanPathogenic GRCh37 chr15: 23,208,842-28,525,460 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 , GRCh38.p12 chr15: 23,319,714-28,280,314 SNORD115-27, LOC105370747, 246 more genes
    nsv5200365copy number variation1nstd102humanPathogenic GRCh37 chr15: 30,652,489-32,438,943 , GRCh38.p12 chr15: 30,360,286-32,146,742 LOC105376704, RN7SL82P, 38 more genes
    nsv5005246copy number variation1nstd200human GRCh38 chr15: 31,391,480-31,392,864 , GRCh37.p13 chr15: 31,683,683-31,685,067 KLF13, LOC105370939
    nsv5001126copy number variation1nstd200human GRCh38 chr15: 31,391,593-31,392,806 , GRCh37.p13 chr15: 31,683,796-31,685,009 LOC105370939, KLF13
    nsv4863723copy number variation1nstd200human GRCh37 chr15: 31,683,695-31,685,040 , GRCh38.p12 chr15: 31,391,492-31,392,837 , GRCh38.p12 chr15|NT_187660.1: 3,677,330-3,678,669 , GRCh38.p12 chr15|NW_011332701.1: 3,564,878-3,566,217 KLF13, LOC105370939
    nsv4855766copy number variation1nstd200human GRCh37 chr15: 32,198,800-32,980,907 , GRCh38.p12 chr15: 31,906,597-32,688,706 , GRCh38.p12 chr15|NT_187660.1: 2,721,314-4,903,294 , GRCh38.p12 chr15|NW_011332701.1: 4,079,283-4,740,842 , LINC02352, 68 more genes
    nsv4762709inversion1nstd199human GRCh37 chr15: 30,618,379-32,496,498 , GRCh38.p12 chr15: 30,326,176-32,204,297 , CHRNA7, 45 more genes
    nsv4761962inversion1nstd199human GRCh37 chr15: 30,668,425-32,446,995 , GRCh38.p12 chr15: 30,376,222-32,154,794 , CHRNA7, 41 more genes
    nsv4753266inversion1nstd199human GRCh37 chr15: 30,605,851-32,517,236 , GRCh38.p12 chr15: 30,313,648-32,225,035 , CHRNA7, 45 more genes
    nsv4749247copy number variation1nstd199human GRCh37 chr15: 29,159,443-34,700,525 , GRCh38.p12 chr15: 28,914,297-34,408,324 , GRCh38.p12 chr15|NT_187660.1: 1,192,197-5,161,414 , GRCh38.p12 chr15|NW_011332701.1: 1,079,713-4,998,962 , HNRNPA1P71, 132 more genes
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