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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099255copy number variation1nstd231human GRCh38.p12 chr1: 192,358,641-201,911,882 , GRCh37 chr1: 192,327,771-201,881,010 CACNA1S, CSRP1, 120 more genes
    nsv7095955copy number variation1nstd102humanUncertain significance GRCh37 chr1: 200,522,516-206,945,780 , GRCh38.p12 chr1: 200,553,388-206,772,435 ELF3, MAPKAPK2, 189 more genes
    nsv7095569copy number variation2nstd102humanUncertain significance GRCh37 chr1: 200,522,516-208,391,267 , GRCh38.p12 chr1: 200,553,388-208,217,922 TRK-TTT8-1, ADIPOR1, 228 more genes
    nsv7057309inversion1nstd229human GRCh38 chr1: 200,648,151-200,816,247 , GRCh37.p13 chr1: 200,617,279-200,785,375 CAMSAP2, DDX59, 1 more genes
    nsv7055522inversion1nstd229human GRCh38 chr1: 200,567,541-200,690,359 , GRCh37.p13 chr1: 200,536,669-200,659,487 KIF14, DDX59, 1 more genes
    nsv6674368copy number variation1nstd229human GRCh38 chr1: 200,683,344-200,686,267 , GRCh37.p13 chr1: 200,652,472-200,655,395 DDX59-AS1
    nsv6672612copy number variation1nstd229human GRCh38 chr1: 200,655,876-200,688,163 , GRCh37.p13 chr1: 200,625,004-200,657,291 DDX59-AS1, DDX59
    nsv6669436copy number variation1nstd229human GRCh38 chr1: 200,480,586-200,711,630 , GRCh37.p13 chr1: 200,449,714-200,680,758 KIF14, DDX59, 2 more genes
    nsv6668471copy number variation1nstd229human GRCh38 chr1: 200,676,164-200,676,532 , GRCh37.p13 chr1: 200,645,292-200,645,660 DDX59-AS1
    nsv6666668copy number variation1nstd229human GRCh38 chr1: 200,673,480-200,682,690 , GRCh37.p13 chr1: 200,642,608-200,651,818 DDX59-AS1
    nsv6664233copy number variation1nstd229human GRCh38 chr1: 200,592,313-200,709,632 , GRCh37.p13 chr1: 200,561,441-200,678,760 DDX59-AS1, KIF14, 1 more genes
    nsv6663649copy number variation1nstd229human GRCh38 chr1: 200,693,870-200,693,928 , GRCh37.p13 chr1: 200,662,998-200,663,056 DDX59-AS1
    nsv6661110copy number variation1nstd229human GRCh38 chr1: 200,686,928-200,690,583 , GRCh37.p13 chr1: 200,656,056-200,659,711 DDX59-AS1
    nsv6636965copy number variation1nstd102humanPathogenic GRCh37 chr1: 181,453,460-213,107,248 , GRCh38.p12 chr1: 181,484,324-212,933,906 PRELP, SYT14, 527 more genes
    nsv6634372copy number variation1nstd102humanPathogenic GRCh37 chr1: 197,867,914-249,224,684 , GRCh38.p12 chr1: 197,898,784-248,930,485 LOC105373279, YBX1P9, 1036 more genes
    nsv6553068inversion1nstd223human GRCh38 chr1: 200,689,804-200,690,449 , GRCh37.p13 chr1: 200,658,932-200,659,577 DDX59-AS1
    nsv6551852inversion1nstd223human GRCh38 chr1: 200,676,369-200,677,313 , GRCh37.p13 chr1: 200,645,497-200,646,441 DDX59-AS1
    nsv6551338inversion1nstd223human GRCh38 chr1: 200,687,345-200,687,785 , GRCh37.p13 chr1: 200,656,473-200,656,913 DDX59-AS1
    nsv6535842inversion1nstd223human GRCh38 chr1: 200,678,010-200,678,648 , GRCh37.p13 chr1: 200,647,138-200,647,776 DDX59-AS1
    nsv6328417copy number variation1nstd223human GRCh38 chr1: 200,685,159-200,686,037 , GRCh37.p13 chr1: 200,654,287-200,655,165 DDX59-AS1
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