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Items: 1 to 20 of 121

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6811560copy number variation1nstd229human GRCh38 chr7: 20,259,751-20,417,539 , GRCh37.p13 chr7: 20,299,374-20,457,162 LOC101927769, ITGB8, 1 more genes
    nsv6804673copy number variation1nstd229human GRCh38 chr7: 20,236,140-20,354,477 , GRCh37.p13 chr7: 20,275,763-20,394,100 ITGB8, ITGB8-AS1, 1 more genes
    nsv6803239copy number variation1nstd229human GRCh38 chr7: 19,777,616-20,444,103 , GRCh37.p13 chr7: 19,817,239-20,483,726 MACC1, ITGB8, 9 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
    nsv6632113copy number variation1nstd224human GRCh37 chr7: 20,319,981-20,376,018 , GRCh38.p12 chr7: 20,280,358-20,336,395 LOC101927769, ITGB8-AS1, 1 more genes
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6313854copy number variation1nstd102humanPathogenic GRCh37 chr7: 9,358,316-20,982,082 , GRCh38.p12 chr7: 9,318,686-20,942,463 LOC107986766, RPL36AP26, 115 more genes
    nsv6313493copy number variation1nstd102humanLikely pathogenic GRCh37 chr7: 10,745,750-35,305,167 , GRCh38.p12 chr7: 10,706,123-35,265,556 ADCYAP1R1, AHR, 329 more genes
    nsv6136985copy number variation1nstd213human GRCh37 chr7: 20,170,000-22,450,001 , GRCh38.p12 chr7: 20,130,377-22,410,382 DNAH11, RAPGEF5, 23 more genes
    nsv6135985copy number variation1nstd213human GRCh37 chr7: 19,600,000-21,460,001 , GRCh38.p12 chr7: 19,560,377-21,420,383 RNU1-15P, ABCB5, 23 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
    nsv4953465copy number variation1nstd200human GRCh38 chr7: 20,236,140-20,354,477 , GRCh37.p13 chr7: 20,275,763-20,394,100 ITGB8-AS1, LOC101927769, 1 more genes
    nsv4882608inversion1nstd200human GRCh37 chr7: 6,326,174-37,121,976 , GRCh38.p12 chr7: 6,286,543-37,082,371 , HOXA13, 435 more genes
    nsv4768371copy number variation1nstd102humanPathogenic GRCh37 chr7: 14,470,668-20,385,165 , GRCh38.p12 chr7: 14,431,043-20,345,542 HDAC9, LOC101927668, 60 more genes
    nsv4455091copy number variation1nstd102humanPathogenic GRCh37 chr7: 10,365-159,119,707 , GRCh38.p12 chr7: 10,365-159,327,017 RPL23AP51, FLJ40288, 2684 more genes
    nsv4139828copy number variation1nstd166human GRCh37.p13 chr7: 19,132,974-20,624,922 , GRCh38.p12 chr7: 19,093,351-20,585,299 LOC101927769, LOC105375181, 18 more genes
    nsv3922488copy number variation1nstd102humanPathogenic GRCh37 chr7: 16,161,141-20,647,522 , GRCh38 chr7: 16,121,516-20,607,899 , NCBI36 chr7: 16,127,666-20,614,047 HDAC9, LOC105375168, 53 more genes
    nsv3922329copy number variation1nstd102humanPathogenic GRCh37 chr7: 43,360-27,236,023 , GRCh38 chr7: 43,360-27,196,404 , NCBI36 chr7: 138,443-27,202,548 LOC401312, IQCE, 411 more genes
    nsv3920312copy number variation1nstd102humanUncertain significance GRCh38 chr7: 18,660,228-20,666,885 , NCBI36 chr7: 18,666,376-20,673,033 , GRCh37 chr7: 18,699,851-20,706,508 NPM1P13, LOC101927769, 24 more genes
    nsv3919826copy number variation1nstd102humanPathogenic GRCh37 chr7: 54,185-159,075,079 , GRCh38 chr7: 54,185-159,282,390 , NCBI36 chr7: 149,268-158,767,840 RNU6-438P, LOC105375300, 2682 more genes
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