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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5922010copy number variation1nstd209human GRCh38 chr8: 86,128,277-86,156,834 , GRCh37.p13 chr8: 87,140,506-87,169,063 ATP6V0D2
    nsv5866334copy number variation1nstd209human GRCh38 chr8: 86,128,284-86,156,729 , GRCh37.p13 chr8: 87,140,513-87,168,958 ATP6V0D2
    nsv5725129mobile element insertion2nstd211human GRCh38 chr8: 86,148,139-86,148,139 , GRCh37.p13 chr8: 87,160,368-87,160,368 ATP6V0D2
    nsv5695351mobile element insertion2nstd211human GRCh38 chr8: 86,134,945-86,134,945 , GRCh37.p13 chr8: 87,147,174-87,147,174 ATP6V0D2
    nsv5578343copy number variation1nstd207human GRCh38 chr8: 86,145,205-86,145,254 , GRCh37.p13 chr8: 87,157,434-87,157,483 ATP6V0D2
    nsv5572211copy number variation1nstd207human GRCh38 chr8: 86,145,180-86,145,282 , GRCh37.p13 chr8: 87,157,409-87,157,511 ATP6V0D2
    nsv5488118copy number variation1nstd206human GRCh38 chr8: 86,100,237-86,101,128 , GRCh37.p13 chr8: 87,112,466-87,113,357 ATP6V0D2
    nsv5487884copy number variation1nstd206human GRCh38 chr8: 86,126,261-86,126,335 , GRCh37.p13 chr8: 87,138,490-87,138,564 ATP6V0D2
    nsv5485288copy number variation1nstd206human GRCh38 chr8: 86,133,063-86,133,118 , GRCh37.p13 chr8: 87,145,292-87,145,347 ATP6V0D2
    nsv5482385copy number variation1nstd206human GRCh38 chr8: 86,118,353-86,118,723 , GRCh37.p13 chr8: 87,130,582-87,130,952 ATP6V0D2
    nsv5480914copy number variation1nstd206human GRCh38 chr8: 86,098,198-86,098,258 , GRCh37.p13 chr8: 87,110,427-87,110,487 ATP6V0D2
    nsv5403561mobile element insertion1nstd206human GRCh38 chr8: 86,134,945-86,134,996 , GRCh37.p13 chr8: 87,147,174-87,147,225 ATP6V0D2
    nsv5371922translocation1nstd200human GRCh38 chr8: 86,126,234-86,126,234 , GRCh38 chr8: 86,126,285-86,126,285 , GRCh37.p13 chr8: 87,138,463-87,138,463 , GRCh37.p13 chr8: 87,138,514-87,138,514 ATP6V0D2
    nsv5364293translocation1nstd200human GRCh38 chr8: 86,134,252-86,134,252 , GRCh38 chr8: 85,907,234-85,907,234 , GRCh37.p13 chr8: 87,146,481-87,146,481 , GRCh37.p13 chr8: 86,919,463-86,919,463 ATP6V0D2
    nsv5315026copy number variation1nstd204human GRCh38.p13 chr8: 86,118,347-86,118,728 , GRCh37.p13 chr8: 87,130,576-87,130,957 ATP6V0D2
    nsv5109736mobile element insertion1nstd203human GRCh38 chr8: 86,140,500-86,140,516 , GRCh37.p13 chr8: 87,152,729-87,152,745 ATP6V0D2
    nsv5036483inversion1nstd200human GRCh38 chr8: 71,454,844-121,935,245 , GRCh37.p13 chr8: 72,367,079-122,947,484 , LINC01617, 636 more genes
    nsv5035989inversion1nstd200human GRCh38 chr8: 74,949,087-131,777,713 , GRCh37.p13 chr8: 75,861,322-132,789,960 , MIR7705, 715 more genes
    nsv4967570copy number variation1nstd200human GRCh38 chr8: 86,152,724-86,168,069 , GRCh37.p13 chr8: 87,164,953-87,180,298 ATP6V0D2
    nsv4967569copy number variation1nstd200human GRCh38 chr8: 86,129,893-86,129,957 , GRCh37.p13 chr8: 87,142,122-87,142,186 ATP6V0D2
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