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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099184copy number variation1nstd231human GRCh38.p12 chr1: 21,486,574-23,087,716 , GRCh37 chr1: 21,813,067-23,414,209 ALPL, C1QA, 36 more genes
    nsv7095949copy number variation1nstd102humanUncertain significance GRCh37 chr1: 19,199,339-24,690,861 , GRCh38.p12 chr1: 18,872,845-24,364,371 RPL29P6, NBPF3, 156 more genes
    nsv7044837inversion1nstd229human GRCh38 chr1: 22,748,739-22,748,861 , GRCh37.p13 chr1: 23,075,232-23,075,354 EPHB2
    nsv7044760inversion1nstd229human GRCh38 chr1: 22,155,852-26,348,296 , GRCh37.p13 chr1: 22,482,345-26,674,787 MIR4684, PDIK1L, 120 more genes
    nsv7039300inversion1nstd229human GRCh38 chr1: 22,796,165-22,798,071 , GRCh37.p13 chr1: 23,122,658-23,124,564 EPHB2
    nsv6647527copy number variation1nstd229human GRCh38 chr1: 22,855,891-22,934,233 , GRCh37.p13 chr1: 23,182,384-23,260,726 MIR4253, EPHB2
    nsv6647526copy number variation1nstd229human GRCh38 chr1: 22,817,545-22,823,007 , GRCh37.p13 chr1: 23,144,038-23,149,500 EPHB2
    nsv6647525copy number variation1nstd229human GRCh38 chr1: 22,772,076-22,775,370 , GRCh37.p13 chr1: 23,098,569-23,101,863 EPHB2
    nsv6647524copy number variation1nstd229human GRCh38 chr1: 22,753,064-22,753,089 , GRCh37.p13 chr1: 23,079,557-23,079,582 EPHB2
    nsv6647523copy number variation1nstd229human GRCh38 chr1: 22,726,147-22,729,826 , GRCh37.p13 chr1: 23,052,640-23,056,319 EPHB2
    nsv6647467copy number variation1nstd229human GRCh38 chr1: 22,892,540-22,892,920 , GRCh37.p13 chr1: 23,219,033-23,219,413 EPHB2
    nsv6647466copy number variation1nstd229human GRCh38 chr1: 22,797,701-22,805,900 , GRCh37.p13 chr1: 23,124,194-23,132,393 EPHB2
    nsv6647465copy number variation1nstd229human GRCh38 chr1: 22,770,323-22,776,739 , GRCh37.p13 chr1: 23,096,816-23,103,232 EPHB2
    nsv6647464copy number variation1nstd229human GRCh38 chr1: 22,749,161-22,757,494 , GRCh37.p13 chr1: 23,075,654-23,083,987 EPHB2
    nsv6647462copy number variation1nstd229human GRCh38 chr1: 22,717,247-22,717,276 , GRCh37.p13 chr1: 23,043,740-23,043,769 EPHB2
    nsv6647460copy number variation1nstd229human GRCh38 chr1: 22,705,417-22,918,776 , GRCh37.p13 chr1: 23,031,910-23,245,269 MIR4684, MIR4253, 1 more genes
    nsv6647457copy number variation1nstd229human GRCh38 chr1: 22,622,346-22,708,970 , GRCh37.p13 chr1: 22,948,839-23,035,463 C1QA, C1QB, 3 more genes
    nsv6647393copy number variation1nstd229human GRCh38 chr1: 22,828,074-22,834,006 , GRCh37.p13 chr1: 23,154,567-23,160,499 EPHB2
    nsv6647392copy number variation1nstd229human GRCh38 chr1: 22,827,024-22,827,226 , GRCh37.p13 chr1: 23,153,517-23,153,719 EPHB2
    nsv6647389copy number variation1nstd229human GRCh38 chr1: 22,701,099-22,741,834 , GRCh37.p13 chr1: 23,027,592-23,068,327 EPHB2, MIR4684
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