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Items: 1 to 20 of 349

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5661181insertion1nstd207human GRCh38 chr11: 530,755-530,755 , GRCh37.p13 chr11: 530,755-530,755 , HRAS, 1 more genes
    nsv5660949insertion1nstd207human GRCh38 chr11: 530,503-530,503 , GRCh37.p13 chr11: 530,503-530,503 , HRAS, 1 more genes
    nsv5658300insertion1nstd207human GRCh38 chr11: 531,138-531,138 , GRCh37.p13 chr11: 531,138-531,138 , HRAS, 1 more genes
    nsv5656475insertion1nstd207human GRCh38 chr11: 530,502-530,502 , GRCh37.p13 chr11: 530,502-530,502 , HRAS, 1 more genes
    nsv5655947insertion1nstd207human GRCh38 chr11: 530,858-530,858 , GRCh37.p13 chr11: 530,858-530,858 , HRAS, 1 more genes
    nsv5653903insertion1nstd207human GRCh38 chr11: 530,550-530,550 , GRCh37.p13 chr11: 530,550-530,550 , HRAS, 1 more genes
    nsv5648265insertion1nstd207human GRCh38 chr11: 531,006-531,006 , GRCh37.p13 chr11: 531,006-531,006 , HRAS, 1 more genes
    nsv5644775insertion1nstd207human GRCh38 chr11: 530,979-530,979 , GRCh37.p13 chr11: 530,979-530,979 , HRAS, 1 more genes
    nsv5603558copy number variation1nstd207human GRCh38 chr11: 530,923-530,978 , GRCh37.p13 chr11: 530,923-530,978 , HRAS, 1 more genes
    nsv5564369copy number variation1nstd102humanUncertain significance GRCh37 chr11: 532,636-533,622 , GRCh38.p12 chr11: 532,636-533,622 , GRCh38.p12 chr11|NT_187586.1: 62,277-63,263 LRRC56, HRAS
    nsv5557461sequence alteration1nstd206human GRCh38 chr11: 428,013-744,860 , GRCh37.p13 chr11: 428,013-744,860 , DRD4, 21 more genes
    nsv5380886copy number variation1nstd102humanUncertain significance GRCh37 chr11: 532,630-532,761 , GRCh38.p12 chr11: 532,630-532,761 , GRCh38.p12 chr11|NT_187586.1: 62,271-62,402 LRRC56, HRAS
    nsv5380885copy number variation1nstd102humanUncertain significance GRCh37 chr11: 298,501-4,113,028 , GRCh38.p12 chr11: 298,501-4,091,798 LINC02688, MIR210, 156 more genes
    nsv5258461copy number variation1nstd204human GRCh38.p13 chr11: 520,301-974,900 , GRCh37.p13 chr11: 520,301-974,900 , SCT, 33 more genes
    nsv5248917copy number variation1nstd204human GRCh38.p13 chr11: 322,701-664,500 , GRCh37.p13 chr11: 322,701-664,500 , ANO9, 23 more genes
    nsv5247998copy number variation1nstd204human GRCh38.p13 chr11: 520,301-585,200 , GRCh37.p13 chr11: 520,301-585,200 , MIR210HG, 8 more genes
    nsv5241692copy number variation1nstd204human GRCh38.p13 chr11: 520,301-530,600 , GRCh37.p13 chr11: 520,301-530,600 , HRAS, 1 more genes
    nsv4769296copy number variation1nstd102humanUncertain significance GRCh37 chr11: 532,631-534,375 , GRCh38.p12 chr11: 532,631-534,375 , GRCh38.p12 chr11|NT_187586.1: 62,272-64,016 HRAS, LRRC56
    nsv4768373copy number variation1nstd102humanPathogenic GRCh37 chr11: 210,300-8,664,358 , GRCh38.p12 chr11: 210,300-8,642,811 LOC107984302, STK33, 375 more genes
    nsv4729665copy number variation1nstd102humanUncertain significance GRCh37 chr11: 230,615-1,150,353 , GRCh38.p12 chr11: 230,615-1,156,726 CD151, RPLP2, 57 more genes
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