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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
    nsv7095680copy number variation1nstd102humanUncertain significance GRCh37 chr1: 100,316,599-100,488,032 , GRCh38.p12 chr1: 99,851,043-100,022,476 AGL, RNU6-750P, 2 more genes
    nsv7095303copy number variation1nstd102humanPathogenic GRCh37 chr1: 100,436,083-100,477,099 , GRCh38.p12 chr1: 99,970,527-100,011,543 RNU6-1318P, RNU6-750P, 1 more genes
    nsv7095301copy number variation1nstd102humanPathogenic GRCh37 chr1: 100,316,589-100,483,381 , GRCh38.p12 chr1: 99,851,033-100,017,825 SLC35A3, RNU6-750P, 2 more genes
    nsv6658086copy number variation1nstd229human GRCh38 chr1: 99,970,225-99,977,699 , GRCh37.p13 chr1: 100,435,781-100,443,255 SLC35A3, RNU6-750P
    nsv6658070copy number variation1nstd229human GRCh38 chr1: 99,966,401-99,987,000 , GRCh37.p13 chr1: 100,431,957-100,452,556 SLC35A3, RNU6-750P
    nsv6657977copy number variation1nstd229human GRCh38 chr1: 99,642,179-100,077,061 , GRCh37.p13 chr1: 100,107,735-100,542,617 MFSD14A, SLC35A3, 8 more genes
    nsv6657975copy number variation1nstd229human GRCh38 chr1: 99,498,947-100,487,486 , GRCh37.p13 chr1: 99,964,503-100,953,042 CDC14A, AGL, 21 more genes
    nsv6657894copy number variation1nstd229human GRCh38 chr1: 99,356,330-99,995,147 , GRCh37.p13 chr1: 99,821,886-100,460,703 LOC107985093, LINC01708, 8 more genes
    nsv6657533copy number variation1nstd229human GRCh38 chr1: 99,985,701-99,994,700 , GRCh37.p13 chr1: 100,451,257-100,460,256 SLC35A3
    nsv6657529copy number variation1nstd229human GRCh38 chr1: 99,931,502-100,193,663 , GRCh37.p13 chr1: 100,397,058-100,659,219 DBT, TRMT13, 6 more genes
    nsv6657528copy number variation1nstd229human GRCh38 chr1: 99,924,501-100,058,000 , GRCh37.p13 chr1: 100,390,057-100,523,556 RNU6-1318P, MFSD14A, 3 more genes
    nsv6638312copy number variation1nstd229human GRCh38 chr1: 100,022,572-100,022,731 , GRCh37.p13 chr1: 100,488,128-100,488,287 SLC35A3
    nsv6638310copy number variation1nstd229human GRCh38 chr1: 100,005,801-100,012,400 , GRCh37.p13 chr1: 100,471,357-100,477,956 SLC35A3
    nsv6638236copy number variation1nstd229human GRCh38 chr1: 100,020,801-100,030,000 , GRCh37.p13 chr1: 100,486,357-100,495,556 SLC35A3
    nsv6638162copy number variation1nstd229human GRCh38 chr1: 100,033,710-100,034,472 , GRCh37.p13 chr1: 100,499,266-100,500,028 SLC35A3
    nsv6638088copy number variation1nstd229human GRCh38 chr1: 100,029,368-100,034,054 , GRCh37.p13 chr1: 100,494,924-100,499,610 SLC35A3
    nsv6551901inversion1nstd223human GRCh38 chr1: 99,983,517-99,983,914 , GRCh37.p13 chr1: 100,449,073-100,449,470 SLC35A3
    nsv6538843inversion1nstd223human GRCh38 chr1: 100,015,010-100,016,123 , GRCh37.p13 chr1: 100,480,566-100,481,679 SLC35A3
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