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Items: 1 to 20 of 207

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5952503insertion1nstd209human GRCh38 chr7: 94,275,728-94,275,728 , GRCh37.p13 chr7: 93,905,040-93,905,040 LOC112267858
    nsv5927485copy number variation1nstd209human GRCh38 chr7: 94,329,020-94,329,331 , GRCh37.p13 chr7: 93,958,332-93,958,643 LOC112267858, LOC107986821
    nsv5693351mobile element insertion1nstd211human GRCh38 chr7: 94,315,804-94,315,804 , GRCh37.p13 chr7: 93,945,116-93,945,116 LOC112267858, LOC107986821
    nsv5629911insertion1nstd207human GRCh38 chr7: 94,275,728-94,275,728 , GRCh37.p13 chr7: 93,905,040-93,905,040 LOC112267858
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5493045copy number variation1nstd206human GRCh38 chr7: 94,297,846-94,297,896 , GRCh37.p13 chr7: 93,927,158-93,927,208 LOC112267858
    nsv5487116copy number variation1nstd206human GRCh38 chr7: 94,343,666-94,347,637 , GRCh37.p13 chr7: 93,972,978-93,976,949 LOC112267858, LOC107986821
    nsv5479366copy number variation1nstd206human GRCh38 chr7: 94,329,031-94,329,332 , GRCh37.p13 chr7: 93,958,343-93,958,644 LOC107986821, LOC112267858
    nsv5405195mobile element insertion1nstd206human GRCh38 chr7: 94,315,804-94,315,855 , GRCh37.p13 chr7: 93,945,116-93,945,167 LOC112267858, LOC107986821
    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
    nsv5370802translocation1nstd200human GRCh38 chr7: 94,353,037-94,353,037 , GRCh38 chr7: 94,352,822-94,352,822 , GRCh37.p13 chr7: 93,982,134-93,982,134 , GRCh37.p13 chr7: 93,982,349-93,982,349 LOC112267858
    nsv5370801translocation1nstd200human GRCh38 chr7: 94,343,666-94,343,666 , GRCh38 chr7: 94,347,637-94,347,637 , GRCh37.p13 chr7: 93,972,978-93,972,978 , GRCh37.p13 chr7: 93,976,949-93,976,949 LOC112267858, LOC107986821
    nsv5321926inversion1nstd204human GRCh37.p13 chr7: 93,899,155-99,360,080 , GRCh38.p13 chr7: 94,269,843-99,762,457 , CYP3A51P, 118 more genes
    nsv5104395mobile element insertion1nstd203human GRCh38 chr7: 94,315,793-94,315,804 , GRCh37.p13 chr7: 93,945,105-93,945,116 LOC112267858, LOC107986821
    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
    nsv4957713copy number variation1nstd200human GRCh38 chr7: 94,355,314-94,355,378 , GRCh37.p13 chr7: 93,984,626-93,984,690 LOC112267858
    nsv4957712copy number variation1nstd200human GRCh38 chr7: 94,301,179-94,301,336 , GRCh37.p13 chr7: 93,930,491-93,930,648 LOC112267858
    nsv4893192mobile element deletion1nstd200human GRCh38 chr7: 94,329,031-94,329,332 , GRCh37.p13 chr7: 93,958,343-93,958,644 LOC112267858, LOC107986821
    nsv4880762inversion1nstd200human GRCh37 chr7: 79,317,862-147,370,680 , GRCh38.p12 chr7: 79,688,546-147,673,588 , RN7SKP277, 1168 more genes
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