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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7053887inversion1nstd229human GRCh38 chr7: 74,171,934-74,839,189 , GRCh37.p13 chr7|NW_003871064.1: 1,701,170-2,368,425 , GRCh37.p13 chr7: 73,586,264-74,223,814 LOC107986742, GTF2IRD1, 13 more genes
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6613731copy number variation1nstd223human GRCh38 chr7: 74,844,801-74,846,200 , GRCh37.p13 chr7|NW_003871064.1: 2,374,037-2,375,436 GTF2IRD2
    nsv6315397copy number variation1nstd102humanPathogenic GRCh37 chr7: 72,589,515-74,629,034 , GRCh38.p12 chr7: 73,175,475-75,175,451 MIR10525, GTF2I, 52 more genes
    nsv6315339copy number variation1nstd102humanPathogenic GRCh37 chr7: 72,589,195-74,225,562 , GRCh38.p12 chr7: 73,175,155-74,809,477 ELN, LIMK1, 44 more genes
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6302452copy number variation1nstd186human GRCh37 chr7: 74,241,664-74,247,684 , GRCh38.p12 chr7: 74,827,891-74,832,561 GTF2IRD2
    nsv6142945copy number variation1nstd206human GRCh38 chr7: 74,807,000-74,815,594 , GRCh37.p13 chr7|NW_003871064.1: 2,336,236-2,344,830 GTF2IRD2
    nsv6141728copy number variation1nstd206human GRCh38 chr7: 74,834,889-74,842,950 , GRCh37.p13 chr7|NW_003871064.1: 2,364,125-2,372,186 GTF2IRD2
    nsv6141719copy number variation1nstd206human GRCh37.p13 chr7|NW_003871064.1: 2,269,836-2,374,015 , GRCh38 chr7: 74,740,600-74,844,779 , GRCh37.p13 chr7: 74,154,935-74,223,814 GTF2IRD2, GTF2I, 2 more genes
    nsv6141571copy number variation1nstd206human GRCh38 chr7: 74,807,439-74,813,139 , GRCh37.p13 chr7|NW_003871064.1: 2,336,675-2,342,375 GTF2IRD2
    nsv6136201copy number variation1nstd213human GRCh37 chr7: 72,600,000-74,410,001 , GRCh38.p12 chr7: 73,185,960-74,984,489 GTF2I, EIF4H, 49 more genes
    nsv5974071inversion1nstd209human GRCh37.p13 chr7|NW_003871064.1: 478,880-2,946,547 , GRCh38 chr7: 72,949,644-75,417,311 , CLDN4, 79 more genes
    nsv5918891copy number variation1nstd209human GRCh38 chr7: 71,592,506-75,175,408 , GRCh37.p13 chr7|NW_003871064.1: 1-2,704,644 , GRCh37.p13 chr7: 71,935,722-74,527,751 , SPDYE10, 78 more genes
    nsv5850076copy number variation2nstd209human GRCh38 chr7: 74,841,489-74,842,794 , GRCh37.p13 chr7|NW_003871064.1: 2,370,725-2,372,030 GTF2IRD2
    nsv5666565inversion1nstd207human GRCh38 chr7: 73,113,990-75,217,887 , GRCh37.p13 chr7|NW_003871064.1: 643,226-2,747,123 , CLDN4, 57 more genes
    nsv5638443insertion1nstd207human GRCh38 chr7: 74,827,907-74,827,907 , GRCh37.p13 chr7|NW_003871064.1: 2,357,143-2,357,143 GTF2IRD2
    nsv5635890insertion1nstd207human GRCh38 chr7: 74,839,100-74,839,100 , GRCh37.p13 chr7|NW_003871064.1: 2,368,336-2,368,336 GTF2IRD2
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5547545insertion1nstd206human GRCh38 chr7: 74,815,731-74,815,764 , GRCh37.p13 chr7|NW_003871064.1: 2,344,967-2,345,000 GTF2IRD2
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