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Items: 1 to 20 of 136

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6812266copy number variation1nstd229human GRCh38 chr7: 20,304,477-20,315,953 , GRCh37.p13 chr7: 20,344,100-20,355,576 LOC101927769
    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
    nsv6801084copy number variation1nstd229human GRCh38 chr7: 20,093,543-20,306,639 , GRCh37.p13 chr7: 20,133,166-20,346,262 LOC101927769, LOC101927668, 4 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
    nsv6619072copy number variation1nstd223human GRCh38 chr7: 20,297,012-20,297,795 , GRCh37.p13 chr7: 20,336,635-20,337,418 LOC101927769
    nsv6608066copy number variation1nstd223human GRCh38 chr7: 20,294,977-20,295,339 , GRCh37.p13 chr7: 20,334,600-20,334,962 LOC101927769
    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
    nsv4607197copy number variation1nstd183human GRCh37 chr7: 20,308,807-20,354,582 , GRCh38.p12 chr7: 20,269,184-20,314,959 LOC101927769
    nsv4455091copy number variation1nstd102humanPathogenic GRCh37 chr7: 10,365-159,119,707 , GRCh38.p12 chr7: 10,365-159,327,017 RPL23AP51, FLJ40288, 2684 more genes
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