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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7147221insertion1nstd232human GRCh37.p13 chr10: 93,713,630-93,713,630 , GRCh38.p12 chr10: 91,953,873-91,953,873 BTAF1
    nsv7144401copy number variation1nstd232human GRCh37.p13 chr10: 93,768,705-93,768,794 , GRCh38.p12 chr10: 92,008,948-92,009,037 BTAF1
    nsv7143500copy number variation1nstd232human GRCh37.p13 chr10: 93,719,637-93,719,733 , GRCh38.p12 chr10: 91,959,880-91,959,976 BTAF1
    nsv7137211copy number variation1nstd102humanPathogenic GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639 EXOC6, VCL, 1906 more genes
    nsv7137209copy number variation1nstd102humanPathogenic GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639 RNU7-12P, RNU1-65P, 1876 more genes
    nsv7098887copy number variation1nstd102humanPathogenic GRCh37 chr10: 93,249,133-97,616,970 , GRCh38.p12 chr10: 91,489,376-95,857,213 LGI1, LOC107984257, 79 more genes
    nsv7073007inversion1nstd229human GRCh38 chr10: 83,678,437-92,070,274 , GRCh37.p13 chr10: 85,438,193-93,830,031 PPP1R3C, LOC105378415, 157 more genes
    nsv7065381inversion1nstd229human GRCh38 chr10: 83,674,811-92,070,275 , GRCh37.p13 chr10: 85,434,567-93,830,032 LINC01520, RPS27P1, 158 more genes
    nsv6897646copy number variation1nstd229human GRCh38 chr10: 92,020,187-92,023,561 , GRCh37.p13 chr10: 93,779,944-93,783,318 BTAF1
    nsv6897307copy number variation1nstd229human GRCh38 chr10: 91,929,909-92,166,613 , GRCh37.p13 chr10: 93,689,666-93,926,370 BTAF1, SDHCP2, 3 more genes
    nsv6894480copy number variation1nstd229human GRCh38 chr10: 91,919,423-91,922,907 , GRCh37.p13 chr10: 93,679,180-93,682,664 BTAF1
    nsv6886933copy number variation1nstd229human GRCh38 chr10: 92,007,295-92,060,701 , GRCh37.p13 chr10: 93,767,052-93,820,458 BTAF1, CPEB3
    nsv6886062copy number variation1nstd229human GRCh38 chr10: 91,870,968-91,981,432 , GRCh37.p13 chr10: 93,630,725-93,741,189 FGFBP3, BTAF1
    nsv6637868copy number variation1nstd102humanPathogenic GRCh37 chr10: 89,823,147-96,056,941 , GRCh38.p12 chr10: 88,063,390-94,297,184 RPS27P1, RNLS, 118 more genes
    nsv6637584copy number variation1nstd102humanUncertain significance GRCh37 chr10: 93,577,943-93,922,822 , GRCh38.p12 chr10: 91,818,186-92,163,065 EIF4A1P8, CPEB3, 5 more genes
    nsv6620930copy number variation1nstd224human GRCh37 chr10: 93,778,269-93,951,793 , GRCh38.p12 chr10: 92,018,512-92,192,036 CPEB3, SDHCP2, 3 more genes
    nsv6620929copy number variation1nstd224human GRCh37 chr10: 93,412,994-94,014,958 , GRCh38.p12 chr10: 91,653,237-92,255,201 EIF4A1P8, LOC107984253, 11 more genes
    nsv6586700inversion1nstd223human GRCh38 chr10: 91,998,817-91,999,682 , GRCh37.p13 chr10: 93,758,574-93,759,439 BTAF1
    nsv6584829inversion1nstd223human GRCh38 chr10: 91,948,408-91,949,035 , GRCh37.p13 chr10: 93,708,165-93,708,792 BTAF1
    nsv6581378inversion1nstd223human GRCh38 chr10: 91,958,061-91,958,709 , GRCh37.p13 chr10: 93,717,818-93,718,466 BTAF1
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