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Items: 1 to 20 of 158

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6818709copy number variation1nstd229human GRCh38 chr7: 74,993,422-78,510,839 , GRCh37.p13 chr7: 75,921,853-78,140,156 TMEM120A, LOC105375359, 75 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
    nsv6618917copy number variation1nstd223human GRCh38 chr7: 75,156,101-75,158,300 , GRCh37.p13 chr7|NW_003871064.1: 2,685,337-2,687,536 NCF1C
    nsv6609379copy number variation1nstd223human GRCh38 chr7: 75,153,301-75,157,000 , GRCh37.p13 chr7|NW_003871064.1: 2,682,537-2,686,236 NCF1C
    nsv6600186copy number variation1nstd223human GRCh38 chr7: 75,154,474-75,155,389 , GRCh37.p13 chr7|NW_003871064.1: 2,683,710-2,684,625 NCF1C
    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
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6290688copy number variation1nstd102humanPathogenic GRCh38 chr7: 75,058,300-79,083,658 , GRCh37.p13 chr7: 75,921,853-78,712,974 GTF2IP1, TMEM60, 76 more genes
    nsv6142061copy number variation1nstd206human GRCh38 chr7: 75,134,779-75,167,500 , GRCh37.p13 chr7|NW_003871064.1: 2,664,015-2,696,736 NCF1C, GTF2IRD2B
    nsv6141995copy number variation1nstd206human GRCh37.p13 chr7|NW_003871064.1: 2,613,015-2,715,015 , GRCh38 chr7: 75,083,779-75,185,779 , GRCh37.p13 chr7: 74,499,593-74,601,500 GTF2IRD2B, NCF1C, 1 more genes
    nsv6141877copy number variation1nstd206human GRCh38 chr7: 75,116,779-75,158,779 , GRCh37.p13 chr7|NW_003871064.1: 2,646,015-2,688,015 GTF2IRD2B, NCF1C
    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
    nsv5481619copy number variation1nstd206human GRCh38 chr7: 75,154,486-75,155,341 , GRCh37.p13 chr7|NW_003871064.1: 2,683,722-2,684,577 NCF1C
    nsv5220489copy number variation1nstd204human GRCh38.p13 chr7: 75,151,901-75,155,700 , GRCh37.p13 chr7|NW_003871064.1: 2,681,137-2,684,936 NCF1C
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv4763531inversion1nstd199human GRCh37 chr7: 66,769,373-102,019,339 , GRCh38.p12 chr7: 67,304,386-102,378,892 , ACHE, 578 more genes
    nsv4730256inversion12nstd198human GRCh38 chr7: 72,909,603-75,903,316 , GRCh37.p13 chr7|NW_003871064.1: 438,839-3,432,552 , CLDN4, 86 more genes
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