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Items: 1 to 20 of 182

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148181copy number variation1nstd102humanPathogenic GRCh38 chr7: 98,454,022-100,723,798 , GRCh37.p13 chr7: 98,083,334-100,321,421 LAMTOR4, PTCD1, 107 more genes
    nsv7052776inversion1nstd229human GRCh38 chr7: 96,709,838-100,726,550 , GRCh37.p13 chr7: 96,339,150-100,324,173 TMEM225B, PILRB, 141 more genes
    nsv6833782copy number variation1nstd229human GRCh38 chr7: 98,846,126-98,927,990 , GRCh37.p13 chr7: 98,443,749-98,525,613 , GRCh37.p13 chr7|NW_003571041.1: 215,308-297,172 MIR3609, TRRAP, 2 more genes
    nsv6833722copy number variation1nstd229human GRCh38 chr7: 98,860,230-98,865,164 , GRCh37.p13 chr7: 98,457,853-98,462,787 , GRCh37.p13 chr7|NW_003571041.1: 229,412-234,346 TMEM130
    nsv6829094copy number variation1nstd229human GRCh38 chr7: 98,868,494-98,871,110 , GRCh37.p13 chr7: 98,466,117-98,468,733 , GRCh37.p13 chr7|NW_003571041.1: 237,676-240,292 TMEM130
    nsv6829089copy number variation1nstd229human GRCh38 chr7: 98,803,126-98,968,206 , GRCh37.p13 chr7|NW_003571041.1: 172,308-327,774 , GRCh37.p13 chr7: 98,400,749-98,556,215 MIR3609, TRRAP, 2 more genes
    nsv6828132copy number variation1nstd229human GRCh38 chr7: 98,667,290-99,135,243 , GRCh37.p13 chr7: 98,296,602-98,556,215 , GRCh37.p13 chr7|NW_003571041.1: 36,472-327,774 SMURF1, TRRAP, 7 more genes
    nsv6822030copy number variation1nstd229human GRCh38 chr7: 98,865,322-99,195,183 , GRCh37.p13 chr7: 98,556,216-98,792,806 TMEM130, SCARNA28, 6 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
    nsv6616739copy number variation1nstd223human GRCh38 chr7: 98,806,653-99,083,746 , GRCh37.p13 chr7|NW_003571041.1: 175,835-327,774 , GRCh37.p13 chr7: 98,404,276-98,556,215 SMURF1, TMEM130, 5 more genes
    nsv6601597copy number variation1nstd223human GRCh38 chr7: 98,818,047-98,897,592 , GRCh37.p13 chr7|NW_003571041.1: 187,229-266,774 , GRCh37.p13 chr7: 98,415,670-98,495,215 TMEM130, TRRAP, 2 more genes
    nsv6574289inversion1nstd223human GRCh38 chr7: 98,857,176-98,858,395 , GRCh37.p13 chr7|NW_003571041.1: 226,358-227,577 , GRCh37.p13 chr7: 98,454,799-98,456,018 TMEM130
    nsv6564429inversion1nstd223human GRCh38 chr7: 98,857,678-98,858,028 , GRCh37.p13 chr7: 98,455,301-98,455,651 , GRCh37.p13 chr7|NW_003571041.1: 226,860-227,210 TMEM130
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6174987copy number variation1nstd214human GRCh38 chr7: 98,858,074-98,858,145 , GRCh37.p13 chr7|NW_003571041.1: 227,256-227,327 , GRCh37.p13 chr7: 98,455,697-98,455,768 TMEM130
    nsv6135799copy number variation1nstd213human GRCh37 chr7: 97,850,000-98,480,001 , GRCh38.p12 chr7: 98,220,688-98,882,378 TECPR1, TMEM130, 12 more genes
    nsv6135785copy number variation1nstd213human GRCh37 chr7: 76,690,000-99,250,001 , GRCh38.p12 chr7: 77,060,683-99,652,378 , ASNS, 283 more genes
    nsv6101547inversion1nstd212human GRCh38 chr7: 98,453,223-101,264,028 , GRCh37.p13 chr7: 98,082,535-100,907,309 , ACHE, 141 more genes
    nsv6001636copy number variation1nstd212human GRCh38 chr7: 98,863,211-98,863,729 , GRCh37.p13 chr7|NW_003571041.1: 232,393-232,911 , GRCh37.p13 chr7: 98,460,834-98,461,352 TMEM130
    nsv5915859copy number variation1nstd209human GRCh38 chr7: 98,858,074-98,858,145 , GRCh37.p13 chr7: 98,455,697-98,455,768 , GRCh37.p13 chr7|NW_003571041.1: 227,256-227,327 TMEM130
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