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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099218copy number variation1nstd231human GRCh38.p12 chr1: 97,675,411-99,337,233 , GRCh37 chr1: 98,140,967-99,802,789 DPYD, PLPPR4, 11 more genes
    nsv7041760inversion1nstd229human GRCh38 chr1: 98,032,764-98,034,611 , GRCh37.p13 chr1: 98,498,320-98,500,167 MIR137HG
    nsv6658010copy number variation1nstd229human GRCh38 chr1: 98,018,848-98,019,055 , GRCh37.p13 chr1: 98,484,404-98,484,611 MIR137HG
    nsv6658009copy number variation1nstd229human GRCh38 chr1: 98,017,611-98,017,697 , GRCh37.p13 chr1: 98,483,167-98,483,253 MIR137HG
    nsv6657850copy number variation1nstd229human GRCh38 chr1: 98,042,535-98,042,734 , GRCh37.p13 chr1: 98,508,091-98,508,290 MIR137HG
    nsv6636421copy number variation1nstd102humanUncertain significance GRCh37 chr1: 96,492,298-98,945,160 , GRCh38.p12 chr1: 96,026,742-98,479,604 NFU1P2, LOC100419654, 22 more genes
    nsv6544493inversion1nstd223human GRCh38 chr1: 98,018,909-98,020,278 , GRCh37.p13 chr1: 98,484,465-98,485,834 MIR137HG
    nsv6329058copy number variation1nstd223human GRCh38 chr1: 98,009,601-98,010,339 , GRCh37.p13 chr1: 98,475,157-98,475,895 MIR137HG
    nsv6327197copy number variation1nstd223human GRCh38 chr1: 98,013,001-98,013,800 , GRCh37.p13 chr1: 98,478,557-98,479,356 MIR137HG
    nsv6326997copy number variation1nstd223human GRCh38 chr1: 97,998,776-97,999,106 , GRCh37.p13 chr1: 98,464,332-98,464,662 MIR137HG
    nsv6324747copy number variation1nstd223human GRCh38 chr1: 98,004,247-98,004,962 , GRCh37.p13 chr1: 98,469,803-98,470,518 MIR137HG
    nsv6322693copy number variation1nstd223human GRCh38 chr1: 98,023,101-98,025,500 , GRCh37.p13 chr1: 98,488,657-98,491,056 MIR137HG
    nsv6322110copy number variation1nstd223human GRCh38 chr1: 98,036,672-98,037,235 , GRCh37.p13 chr1: 98,502,228-98,502,791 MIR137HG
    nsv6321104copy number variation1nstd223human GRCh38 chr1: 98,023,201-98,024,000 , GRCh37.p13 chr1: 98,488,757-98,489,556 MIR137HG
    nsv6320938copy number variation1nstd223human GRCh38 chr1: 98,029,501-98,030,700 , GRCh37.p13 chr1: 98,495,057-98,496,256 MIR137HG
    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
    nsv6212488insertion2nstd214human GRCh38 chr1: 98,046,177-98,046,177 , GRCh37.p13 chr1: 98,511,733-98,511,733 MIR137HG, MIR137
    nsv6151721copy number variation1nstd214human GRCh38 chr1: 98,027,074-98,027,153 , GRCh37.p13 chr1: 98,492,630-98,492,709 MIR137HG
    nsv6133669copy number variation1nstd213human GRCh37 chr1: 95,900,000-101,030,001 , GRCh38.p12 chr1: 95,434,444-100,564,445 PALMD, LRRC39, 56 more genes
    nsv6046176insertion1nstd212human GRCh38 chr1: 98,046,177-98,046,177 , GRCh37.p13 chr1: 98,511,733-98,511,733 MIR137, MIR137HG
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