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Items: 1 to 20 of 104

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097853copy number variation1nstd102humanPathogenic GRCh37 chr7: 104,456,677-108,155,935 , GRCh38.p12 chr7: 104,816,230-108,515,491 RNU6-1322P, COG5, 57 more genes
    nsv7046492inversion1nstd229human GRCh38 chr7: 108,472,441-108,597,964 , GRCh37.p13 chr7: 108,112,885-108,238,408 PNPLA8, THAP5, 3 more genes
    nsv6837624copy number variation1nstd229human GRCh38 chr7: 108,282,201-108,763,200 , GRCh37.p13 chr7: 107,922,645-108,403,644 DNAJB9, THAP5, 5 more genes
    nsv6828603copy number variation1nstd229human GRCh38 chr7: 107,770,269-108,588,414 , GRCh37.p13 chr7: 107,410,714-108,228,858 LOC105375444, DLD, 15 more genes
    nsv6819404copy number variation1nstd229human GRCh38 chr7: 108,039,939-108,542,564 , GRCh37.p13 chr7: 107,680,384-108,183,008 PNPLA8, RPL7P32, 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
    nsv6616656copy number variation1nstd223human GRCh38 chr7: 108,482,442-108,535,056 , GRCh37.p13 chr7: 108,122,886-108,175,500 PNPLA8, RPL7P32
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6313851copy number variation1nstd102humanPathogenic GRCh37 chr7: 106,984,287-128,949,489 , GRCh38.p12 chr7: 107,343,842-129,309,648 DOCK4-AS1, RPL3P8, 262 more genes
    nsv6313641copy number variation1nstd102humanUncertain significance GRCh37 chr7: 108,099,153-108,503,957 , GRCh38.p12 chr7: 108,458,709-108,863,513 LOC107986836, LOC100419644, 5 more genes
    nsv6313576copy number variation1nstd102humanPathogenic GRCh37 chr7: 100,676,872-119,156,160 , GRCh38.p12 chr7: 101,033,591-119,516,106 LHFPL3-AS2, CTB-30L5.1, 233 more genes
    nsv6313503copy number variation1nstd102humanPathogenic GRCh37 chr7: 99,417,471-111,586,308 , GRCh38.p12 chr7: 99,819,848-111,946,253 GJC3, LAMB4, 237 more genes
    nsv6136536copy number variation1nstd213human GRCh37 chr7: 107,510,000-112,950,001 , GRCh38.p12 chr7: 107,869,555-113,309,946 NPM1P14, LRRN3, 52 more genes
    nsv6136533copy number variation1nstd213human GRCh37 chr7: 104,130,000-120,060,001 , GRCh38.p12 chr7: 104,489,552-120,419,947 CAPZA2, CFTR, 162 more genes
    nsv6135948copy number variation1nstd213human GRCh37 chr7: 105,420,000-108,740,001 , GRCh38.p12 chr7: 105,779,554-109,099,944 NAMPT, COG5, 49 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
    nsv5326600inversion1nstd204human GRCh37.p13 chr7: 97,320,865-141,491,704 , GRCh38.p13 chr7: 97,691,553-141,791,904 , ARF5, 752 more genes
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv5029742inversion1nstd200human GRCh38 chr7: 79,688,546-147,673,588 , GRCh37.p13 chr7: 79,317,862-147,370,680 , LOC100533722, 1168 more genes
    nsv4950737copy number variation1nstd200human GRCh38 chr7: 108,482,447-108,535,006 , GRCh37.p13 chr7: 108,122,891-108,175,450 RPL7P32, PNPLA8
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