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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099219copy number variation1nstd231human GRCh38.p12 chr1: 99,594,616-101,416,026 , GRCh37 chr1: 100,060,172-101,881,582 AGL, DBT, 38 more genes
    nsv7095681copy number variation1nstd102humanUncertain significance GRCh37 chr1: 100,316,599-101,709,564 , GRCh38.p12 chr1: 99,851,043-101,244,008 SLC35A3, S1PR1-DT, 29 more genes
    nsv7044488inversion1nstd229human GRCh38 chr1: 100,052,919-109,025,639 , GRCh37.p13 chr1: 100,518,475-109,568,261 LOC102723784, DNAJA1P5, 109 more genes
    nsv6638339copy number variation1nstd229human GRCh38 chr1: 100,887,401-100,895,200 , GRCh37.p13 chr1: 101,352,957-101,360,756 SLC30A7, EXTL2
    nsv6638332copy number variation1nstd229human GRCh38 chr1: 100,743,298-100,891,889 , GRCh37.p13 chr1: 101,208,854-101,357,445 EXTL2
    nsv6638274copy number variation1nstd229human GRCh38 chr1: 100,861,985-101,202,903 , GRCh37.p13 chr1: 101,327,541-101,668,459 EXTL2, HNRNPA1P68, 4 more genes
    nsv6638269copy number variation1nstd229human GRCh38 chr1: 100,818,530-100,909,625 , GRCh37.p13 chr1: 101,284,086-101,375,181 EXTL2, SLC30A7
    nsv6638183copy number variation1nstd229human GRCh38 chr1: 100,881,501-100,883,000 , GRCh37.p13 chr1: 101,347,057-101,348,556 EXTL2
    nsv6638182copy number variation1nstd229human GRCh38 chr1: 100,868,587-100,871,504 , GRCh37.p13 chr1: 101,334,143-101,337,060 EXTL2
    nsv6638177copy number variation1nstd229human GRCh38 chr1: 100,699,205-101,532,642 , GRCh37.p13 chr1: 101,164,761-101,998,198 S1PR1, LOC101928334, 11 more genes
    nsv6638108copy number variation1nstd229human GRCh38 chr1: 100,722,465-101,015,813 , GRCh37.p13 chr1: 101,188,021-101,481,369 DPH5, VCAM1, 3 more genes
    nsv6313675copy number variation1nstd102humanPathogenic GRCh37 chr1: 95,046,805-114,714,931 , GRCh38.p12 chr1: 94,581,249-114,172,309 LINC01307, FTLP17, 320 more genes
    nsv6290366copy number variation1nstd102humanUncertain significance GRCh37 chr1: 100,215,607-105,368,230 , GRCh38.p12 chr1: 99,750,051-104,825,608 LOC105379827, RPSAP19, 63 more genes
    nsv6133490copy number variation1nstd213human GRCh37 chr1: 101,020,000-101,380,001 , GRCh38.p12 chr1: 100,554,444-100,914,445 EXTL2, VCAM1, 4 more genes
    nsv5418533copy number variation1nstd206human GRCh38 chr1: 100,873,400-100,873,482 , GRCh37.p13 chr1: 101,338,956-101,339,038 EXTL2
    nsv5077418mobile element insertion1nstd203human GRCh38 chr1: 100,891,091-100,891,106 , GRCh37.p13 chr1: 101,356,647-101,356,662 EXTL2
    nsv5063201mobile element insertion1nstd203human GRCh38 chr1: 100,871,263-100,871,281 , GRCh37.p13 chr1: 101,336,819-101,336,837 EXTL2
    nsv5060026copy number variation1nstd102humanUncertain significance GRCh37 chr1: 101,326,711-104,423,819 , GRCh38.p12 chr1: 100,861,155-103,881,197 LOC105378878, RNPC3, 33 more genes
    nsv4788855copy number variation1nstd200human GRCh37 chr1: 101,341,580-101,341,910 , GRCh38.p12 chr1: 100,876,024-100,876,354 EXTL2
    nsv4767860inversion1nstd199human GRCh37 chr1: 17,051,740-234,912,187 , GRCh38.p12 chr1: 16,725,245-234,776,440 , ABCA4, 4269 more genes
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