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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137028copy number variation1nstd102humanPathogenic GRCh38 chr7: 73,214,501-74,773,500 , GRCh37.p13 chr7|NW_003871064.1: 743,737-2,302,736 , GRCh37.p13 chr7: 72,631,166-74,187,847 LOC105375350, NSUN5, 41 more genes
    nsv7098968copy number variation1nstd102humanLikely pathogenic GRCh37 chr7: 74,188,451-74,195,125 , GRCh38.p12 chr7: 74,774,104-74,780,779 NCF1
    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
    nsv6610611copy number variation1nstd223human GRCh38 chr7: 74,771,601-74,773,500 , GRCh37.p13 chr7: 74,185,948-74,187,847 , GRCh37.p13 chr7|NW_003871064.1: 2,300,837-2,302,736 NCF1
    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
    nsv6304859copy number variation1nstd186human GRCh37 chr7: 74,180,345-74,189,126 , GRCh38.p12 chr7: 74,766,000-74,774,779 NCF1
    nsv6142448copy number variation1nstd206human GRCh38 chr7: 74,746,779-74,790,500 , GRCh37.p13 chr7: 74,161,117-74,204,843 , GRCh37.p13 chr7|NW_003871064.1: 2,276,015-2,319,736 NCF1, GTF2I
    nsv6142008copy number variation1nstd206human GRCh38 chr7: 74,766,000-74,774,779 , GRCh37.p13 chr7: 74,180,345-74,189,126 , GRCh37.p13 chr7|NW_003871064.1: 2,295,236-2,304,015 NCF1
    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
    nsv6141525copy number variation1nstd206human GRCh38 chr7: 74,780,779-74,792,889 , GRCh37.p13 chr7: 74,195,125-74,207,231 , GRCh37.p13 chr7|NW_003871064.1: 2,310,015-2,322,125 NCF1
    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
    nsv6008189copy number variation1nstd212human GRCh38 chr7: 74,781,162-74,782,355 , GRCh37.p13 chr7|NW_003871064.1: 2,310,398-2,311,591 , GRCh37.p13 chr7: 74,195,509-74,196,700 NCF1
    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
    nsv5666565inversion1nstd207human GRCh38 chr7: 73,113,990-75,217,887 , GRCh37.p13 chr7|NW_003871064.1: 643,226-2,747,123 , CLDN4, 57 more genes
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5485202copy number variation1nstd206human GRCh38 chr7: 74,784,389-74,814,100 , GRCh37.p13 chr7|NW_003871064.1: 2,313,625-2,343,336 , GRCh37.p13 chr7: 74,198,732-74,223,814 NCF1, GTF2IRD2
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