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Items: 1 to 20 of 163

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv5572794copy number variation1nstd207human 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
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5381780copy number variation1nstd102humanPathogenic GRCh37 chr7: 87,477,185-100,333,327 , GRCh38.p12 chr7: 87,847,870-100,735,704 ARPC1A, LOC112267858, 265 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
    nsv5321926inversion1nstd204human GRCh37.p13 chr7: 93,899,155-99,360,080 , GRCh38.p13 chr7: 94,269,843-99,762,457 , CYP3A51P, 118 more genes
    nsv5311385copy number variation1nstd204human GRCh38.p13 chr7: 98,852,282-98,862,691 , GRCh37.p13 chr7|NW_003571041.1: 221,464-231,873 , GRCh37.p13 chr7: 98,449,905-98,460,314 TMEM130
    nsv5260182copy number variation1nstd204human GRCh38.p13 chr7: 98,852,300-98,861,323 , GRCh37.p13 chr7: 98,449,923-98,458,946 , GRCh37.p13 chr7|NW_003571041.1: 221,482-230,505 TMEM130
    nsv5115237mobile element insertion1nstd203human GRCh38 chr7: 98,861,187-98,861,237 , GRCh37.p13 chr7|NW_003571041.1: 230,369-230,419 , GRCh37.p13 chr7: 98,458,810-98,458,860 TMEM130
    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
    nsv4966644copy number variation1nstd200human GRCh38 chr7: 98,868,494-98,871,110 , GRCh37.p13 chr7|NW_003571041.1: 237,676-240,292 , GRCh37.p13 chr7: 98,466,117-98,468,733 TMEM130
    nsv4880762inversion1nstd200human GRCh37 chr7: 79,317,862-147,370,680 , GRCh38.p12 chr7: 79,688,546-147,673,588 , RN7SKP277, 1168 more genes
    nsv4819714copy number variation1nstd200human GRCh37 chr7: 98,466,117-98,468,733 , GRCh38.p12 chr7: 98,868,494-98,871,110 TMEM130
    nsv4763531inversion1nstd199human GRCh37 chr7: 66,769,373-102,019,339 , GRCh38.p12 chr7: 67,304,386-102,378,892 , ACHE, 578 more genes
    nsv4729043copy number variation1nstd102humanUncertain significance GRCh37 chr7: 98,277,871-98,483,457 , GRCh38.p12 chr7: 98,648,559-98,885,834 MIR3609, LOC105375418, 5 more genes
    nsv4651597copy number variation1nstd186human GRCh37 chr7: 98,460,139-98,460,626 , GRCh38.p12 chr7: 98,862,516-98,863,003 TMEM130
    nsv4610409copy number variation1nstd183human GRCh37 chr7: 98,366,565-98,560,243 , GRCh38.p12 chr7: 98,737,253-98,962,620 TMEM130, MIR3609, 3 more genes
    nsv4456313copy number variation1nstd102humanUncertain significance GRCh37 chr7: 98,373,794-98,676,268 , GRCh38.p12 chr7: 98,744,482-99,078,645 TMEM130, RNU6-393P, 6 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
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