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Items: 1 to 20 of 265

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5922939copy number variation1nstd209human GRCh38 chr7: 64,666,914-64,666,972 , GRCh37.p13 chr7: 64,127,292-64,127,350 ZNF107
    nsv5917265copy number variation1nstd209human GRCh38 chr7: 64,708,187-64,708,270 , GRCh37.p13 chr7: 64,168,565-64,168,648 ZNF107
    nsv5580209copy number variation1nstd207human GRCh38 chr7: 64,666,914-64,666,972 , GRCh37.p13 chr7: 64,127,292-64,127,350 ZNF107
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5487246copy number variation1nstd206human GRCh38 chr7: 64,688,359-64,703,591 , GRCh37.p13 chr7: 64,148,737-64,163,969 ZNF107
    nsv5477471copy number variation1nstd206human GRCh38 chr7: 64,706,818-64,707,282 , GRCh37.p13 chr7: 64,167,196-64,167,660 ZNF107
    nsv5477111copy number variation1nstd206human GRCh38 chr7: 64,666,914-64,666,973 , GRCh37.p13 chr7: 64,127,292-64,127,351 ZNF107
    nsv5475478copy number variation1nstd206human GRCh38 chr7: 64,709,535-64,710,144 , GRCh37.p13 chr7: 64,169,913-64,170,522 ZNF107
    nsv5363778translocation1nstd200human GRCh38 chr7: 64,709,854-64,709,854 , GRCh38 chr7: 64,709,787-64,709,787 , GRCh37.p13 chr7: 64,170,165-64,170,165 , GRCh37.p13 chr7: 64,170,232-64,170,232 ZNF107
    nsv5320871translocation1nstd204human GRCh38.p13 chr2: 47,772,102-47,772,102 , GRCh38.p13 chr7: 64,697,695-64,697,695 , GRCh37.p13 chr2: 47,999,241-47,999,241 , GRCh37.p13 chr7: 64,158,073-64,158,073 ZNF107
    nsv5109423mobile element insertion1nstd203human GRCh38 chr7: 64,709,634-64,709,637 , GRCh37.p13 chr7: 64,170,012-64,170,015 ZNF107
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv4957463copy number variation1nstd200human GRCh38 chr7: 64,688,407-64,725,466 , GRCh37.p13 chr7: 64,148,785-64,185,844 ZNF107
    nsv4957462copy number variation1nstd200human GRCh38 chr7: 64,675,667-64,679,355 , GRCh37.p13 chr7: 64,136,045-64,139,733 ZNF107, MIR6839, 1 more genes
    nsv4957461copy number variation1nstd200human GRCh38 chr7: 64,673,881-64,817,136 , GRCh37.p13 chr7: 64,134,259-64,277,514 BNIP3P11, MIR6839, 3 more genes
    nsv4953961copy number variation1nstd200human GRCh38 chr7: 64,593,451-64,719,460 , GRCh37.p13 chr7: 64,053,829-64,179,838 BNIP3P11, LOC100128885, 3 more genes
    nsv4819325copy number variation1nstd200human GRCh37 chr7: 64,167,198-64,167,684 , GRCh38.p12 chr7: 64,706,820-64,707,306 ZNF107
    nsv4819324copy number variation1nstd200human GRCh37 chr7: 64,148,785-64,185,844 , GRCh38.p12 chr7: 64,688,407-64,725,466 ZNF107
    nsv4819323copy number variation1nstd200human GRCh37 chr7: 64,136,045-64,139,733 , GRCh38.p12 chr7: 64,675,667-64,679,355 ZNF107, MIR6839, 1 more genes
    nsv4761040inversion1nstd199human GRCh37 chr7: 55,830,732-65,288,125 , GRCh38.p12 chr7: 55,763,039-65,823,138 , CCT6A, 247 more genes
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