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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7069370inversion1nstd229human GRCh38 chr8: 74,779,865-81,220,765 , GRCh37.p13 chr8: 75,692,100-82,133,000 THAP12P7, LOC105375905, 69 more genes
    nsv6857526copy number variation1nstd229human GRCh38 chr8: 80,993,883-80,998,406 , GRCh37.p13 chr8: 81,906,118-81,910,641 PAG1
    nsv6856539copy number variation1nstd229human GRCh38 chr8: 81,096,758-81,097,169 , GRCh37.p13 chr8: 82,008,993-82,009,404 PAG1
    nsv6855834copy number variation1nstd229human GRCh38 chr8: 81,078,405-81,081,787 , GRCh37.p13 chr8: 81,990,640-81,994,022 PAG1
    nsv6855734copy number variation1nstd229human GRCh38 chr8: 81,074,655-81,173,224 , GRCh37.p13 chr8: 81,986,890-82,085,459 LOC105375924, PAG1
    nsv6854620copy number variation1nstd229human GRCh38 chr8: 81,068,547-81,071,713 , GRCh37.p13 chr8: 81,980,782-81,983,948 PAG1
    nsv6853812copy number variation1nstd229human GRCh38 chr8: 80,994,055-80,994,132 , GRCh37.p13 chr8: 81,906,290-81,906,367 PAG1
    nsv6853681copy number variation1nstd229human GRCh38 chr8: 80,984,906-81,357,538 , GRCh37.p13 chr8: 81,897,141-82,269,773 LOC105375924, FABP5, 4 more genes
    nsv6853130copy number variation1nstd229human GRCh38 chr8: 81,079,540-81,082,117 , GRCh37.p13 chr8: 81,991,775-81,994,352 PAG1
    nsv6851048copy number variation1nstd229human GRCh38 chr8: 81,044,897-81,054,419 , GRCh37.p13 chr8: 81,957,132-81,966,654 PAG1
    nsv6850315copy number variation1nstd229human GRCh38 chr8: 81,064,653-81,064,691 , GRCh37.p13 chr8: 81,976,888-81,976,926 PAG1
    nsv6850061copy number variation1nstd229human GRCh38 chr8: 81,016,032-81,020,781 , GRCh37.p13 chr8: 81,928,267-81,933,016 PAG1
    nsv6848749copy number variation1nstd229human GRCh38 chr8: 81,075,854-81,079,768 , GRCh37.p13 chr8: 81,988,089-81,992,003 PAG1
    nsv6846979copy number variation1nstd229human GRCh38 chr8: 81,095,046-81,095,236 , GRCh37.p13 chr8: 82,007,281-82,007,471 PAG1
    nsv6844240copy number variation1nstd229human GRCh38 chr8: 80,968,081-80,972,954 , GRCh37.p13 chr8: 81,880,316-81,885,189 PAG1
    nsv6843011copy number variation1nstd229human GRCh38 chr8: 81,031,163-81,035,669 , GRCh37.p13 chr8: 81,943,398-81,947,904 PAG1
    nsv6841543copy number variation1nstd229human GRCh38 chr8: 81,030,895-81,031,081 , GRCh37.p13 chr8: 81,943,130-81,943,316 PAG1
    nsv6636819copy number variation1nstd102humanUncertain significance GRCh37 chr8: 79,876,744-83,112,711 , GRCh38.p12 chr8: 78,964,509-82,200,476 SLC25A51P3, PMP2, 59 more genes
    nsv6636450copy number variation1nstd102humanPathogenic GRCh37 chr8: 79,409,349-119,040,631 , GRCh38.p12 chr8: 78,497,114-118,028,392 MIR2053, RPS2P33, 507 more genes
    nsv6634360copy number variation1nstd102humanPathogenic GRCh37 chr8: 68,912,432-146,295,771 , GRCh38.p12 chr8: 68,000,197-145,070,385 WASHC5, LOC100132280, 1028 more genes
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