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Items: 1 to 20 of 153

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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
    nsv5490456copy number variation1nstd206human GRCh38 chr7: 101,299,786-101,308,468 , GRCh37.p13 chr7: 100,943,067-100,951,749 LNCPRESS1, EMSLR
    nsv5488459copy number variation1nstd206human GRCh38 chr7: 101,297,219-101,304,496 , GRCh37.p13 chr7: 100,940,500-100,947,777 LNCPRESS1
    nsv5370872translocation1nstd200human GRCh38 chr7: 101,299,698-101,299,698 , GRCh38 chr7: 101,302,796-101,302,796 , GRCh37.p13 chr7: 100,942,979-100,942,979 , GRCh37.p13 chr7: 100,946,077-100,946,077 LNCPRESS1
    nsv5326600inversion1nstd204human GRCh37.p13 chr7: 97,320,865-141,491,704 , GRCh38.p13 chr7: 97,691,553-141,791,904 , ARF5, 752 more genes
    nsv5305137copy number variation1nstd204human GRCh38.p13 chr7: 101,300,028-101,303,117 , GRCh37.p13 chr7: 100,943,309-100,946,398 LNCPRESS1
    nsv5260154copy number variation1nstd204human GRCh38.p13 chr7: 101,299,736-101,303,160 , GRCh37.p13 chr7: 100,943,017-100,946,441 LNCPRESS1
    nsv5248813copy number variation1nstd204human GRCh38.p13 chr7: 101,300,801-101,303,200 , GRCh37.p13 chr7: 100,944,082-100,946,481 LNCPRESS1
    nsv5243338copy number variation1nstd204human GRCh37.p13 chr7: 100,908,982-101,094,581 , GRCh38.p13 chr7: 101,265,701-101,451,300 IFT22, COL26A1, 4 more genes
    nsv5242483copy number variation1nstd204human GRCh38.p13 chr7: 101,265,701-101,357,400 , GRCh37.p13 chr7: 100,908,982-101,000,681 IFT22, LNCPRESS1, 3 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
    nsv4966767copy number variation1nstd200human GRCh38 chr7: 101,297,224-101,304,476 , GRCh37.p13 chr7: 100,940,505-100,947,757 LNCPRESS1
    nsv4965058copy number variation1nstd200human GRCh38 chr7: 101,299,341-101,308,245 , GRCh37.p13 chr7: 100,942,622-100,951,526 EMSLR, LNCPRESS1
    nsv4965057copy number variation1nstd200human GRCh38 chr7: 101,291,401-102,143,126 , GRCh37.p13 chr7: 100,934,682-101,718,950 , CUX1, 7 more genes
    nsv4965056copy number variation1nstd200human GRCh38 chr7: 101,283,406-101,305,265 , GRCh37.p13 chr7: 100,926,687-100,948,546 LNCPRESS1, AZGP1P2
    nsv4880762inversion1nstd200human GRCh37 chr7: 79,317,862-147,370,680 , GRCh38.p12 chr7: 79,688,546-147,673,588 , RN7SKP277, 1168 more genes
    nsv4825213copy number variation1nstd200human GRCh37 chr7: 100,942,622-100,951,526 , GRCh38.p12 chr7: 101,299,341-101,308,245 EMSLR, LNCPRESS1
    nsv4819801copy number variation1nstd200human GRCh37 chr7: 100,943,293-100,946,413 , GRCh38.p12 chr7: 101,300,012-101,303,132 LNCPRESS1
    nsv4819800copy number variation1nstd200human GRCh37 chr7: 100,940,505-100,947,757 , GRCh38.p12 chr7: 101,297,224-101,304,476 LNCPRESS1
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