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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5490464copy number variation1nstd206human GRCh38 chr7: 47,574,212-48,050,719 , GRCh37.p13 chr7: 47,613,810-48,090,316 LINC02902, C7orf57, 8 more genes
    nsv5381787copy number variation1nstd102humanPathogenic GRCh37 chr7: 43,341,583-50,171,623 , GRCh38.p12 chr7: 43,301,984-50,132,027 OGDH, LOC112267918, 110 more genes
    nsv5381783copy number variation1nstd102humanPathogenic GRCh37 chr7: 41,124,364-47,945,566 , GRCh38.p12 chr7: 41,084,766-47,905,969 ELK1P1, URGCP, 121 more genes
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv4956546copy number variation1nstd200human GRCh38 chr7: 47,668,908-47,793,878 , GRCh37.p13 chr7: 47,708,506-47,833,476 PKD1L1, LINC00525, 1 more genes
    nsv4953663copy number variation1nstd200human GRCh38 chr7: 47,628,732-47,865,774 , GRCh37.p13 chr7: 47,668,330-47,905,372 PKD1L1, LINC02902, 3 more genes
    nsv4675933copy number variation1nstd102humanUncertain significance GRCh37 chr7: 47,461,423-47,878,993 , GRCh38.p12 chr7: 47,421,825-47,839,395 LINC02902, PKD1L1, 5 more genes
    nsv4664572copy number variation1nstd186human GRCh37 chr7: 47,795,690-47,800,431 , GRCh38.p12 chr7: 47,756,092-47,760,833 LINC00525
    nsv4660296copy number variation2nstd186human GRCh37 chr7: 47,801,119-47,801,180 , GRCh38.p12 chr7: 47,761,521-47,761,582 LINC00525
    nsv4659763copy number variation2nstd186human GRCh37 chr7: 47,800,386-47,801,158 , GRCh38.p12 chr7: 47,760,788-47,761,560 LINC00525
    nsv4618023copy number variation2nstd183human GRCh37 chr7: 47,801,119-47,801,180 , GRCh38.p12 chr7: 47,761,521-47,761,582 LINC00525
    nsv4613150copy number variation1nstd183human GRCh37 chr7: 47,799,598-47,801,468 , GRCh38.p12 chr7: 47,760,000-47,761,870 LINC00525
    nsv4607603copy number variation1nstd183human GRCh37 chr7: 47,801,119-47,804,447 , GRCh38.p12 chr7: 47,761,521-47,764,849 LINC00525
    nsv4606833copy number variation2nstd183human GRCh37 chr7: 47,800,386-47,801,158 , GRCh38.p12 chr7: 47,760,788-47,761,560 LINC00525
    nsv4600650copy number variation2nstd183human GRCh37 chr7: 47,795,690-47,800,431 , GRCh38.p12 chr7: 47,756,092-47,760,833 LINC00525
    nsv4600585copy number variation1nstd183human GRCh37 chr7: 47,801,119-47,814,336 , GRCh38.p12 chr7: 47,761,521-47,774,738 PKD1L1, LINC00525
    nsv4599433copy number variation1nstd183human GRCh37 chr7: 47,800,305-47,800,439 , GRCh38.p12 chr7: 47,760,707-47,760,841 LINC00525
    nsv4524313copy number variation1nstd166human GRCh37.p13 chr7: 47,668,333-47,905,369 , GRCh38.p12 chr7: 47,628,735-47,865,771 LINC00525, LINC02902, 3 more genes
    nsv4456579copy number variation1nstd102humanUncertain significance GRCh37 chr7: 47,709,853-47,834,458 , GRCh38.p12 chr7: 47,670,255-47,794,860 PKD1L1, LINC00525, 1 more genes
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