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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7053197inversion1nstd229human GRCh38 chr7: 72,920,579-74,172,062 , GRCh37.p13 chr7: 72,391,116-73,586,392 , GRCh37.p13 chr7|NW_003871064.1: 449,815-1,701,298 FKBP6, TRIM74, 41 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
    nsv6632373copy number variation1nstd224human GRCh37 chr7: 72,313,144-72,761,178 , GRCh38.p12 chr7: 72,842,566-73,347,179 POM121, TRIM74, 20 more genes
    nsv6612332copy number variation1nstd223human GRCh38 chr7: 73,116,801-73,156,200 , GRCh37.p13 chr7: 72,531,124-72,552,027 , GRCh37.p13 chr7|NW_003871064.1: 646,037-685,436 GTF2IP4, SPDYE10
    nsv6609506copy number variation1nstd223human GRCh38 chr7: 73,200,801-73,202,100 , GRCh37.p13 chr7|NW_003871064.1: 730,037-731,336 GTF2IP4
    nsv6609009copy number variation1nstd223human GRCh38 chr7: 73,189,301-73,194,500 , GRCh37.p13 chr7|NW_003871064.1: 718,537-723,736 GTF2IP4
    nsv6574642inversion1nstd223human GRCh38 chr7: 72,920,579-74,172,062 , GRCh37.p13 chr7|NW_003871064.1: 449,815-1,701,298 , GRCh37.p13 chr7: 72,391,116-73,586,392 CLDN4, TBL2, 41 more genes
    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
    nsv6142561copy number variation1nstd206human GRCh38 chr7: 72,942,389-73,297,889 , GRCh37.p13 chr7|NW_003871064.1: 471,625-827,125 POM121, GTF2IRD2P1, 15 more genes
    nsv6141807copy number variation1nstd206human GRCh38 chr7: 72,698,779-73,300,779 , GRCh37.p13 chr7|NW_003871064.1: 228,028-830,015 PMS2P6, TYW1B, 22 more genes
    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
    nsv6005121copy number variation1nstd212human GRCh38 chr7: 73,189,768-73,190,334 , GRCh37.p13 chr7|NW_003871064.1: 719,004-719,570 GTF2IP4
    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
    nsv5642113insertion1nstd207human GRCh38 chr7: 73,166,838-73,166,838 , GRCh37.p13 chr7|NW_003871064.1: 696,074-696,074 , GRCh37.p13 chr7: 74,855,742-74,855,742 GTF2IP4
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5485948copy number variation1nstd206human GRCh37.p13 chr7|NW_003871064.1: 733,015-826,015 , GRCh38 chr7: 73,203,779-73,296,779 POM121B, NCF1B, 2 more genes
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