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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148198copy number variation1nstd102humanPathogenic GRCh38 chr1: 151,017,715-151,018,767 , GRCh37.p13 chr1: 150,990,191-150,991,243 PRUNE1
    nsv7099231copy number variation1nstd231human GRCh38.p12 chr1: 149,962,894-151,006,586 , GRCh37 chr1: 149,934,818-150,979,062 ARNT, CTSK, 48 more genes
    nsv7056211inversion1nstd229human GRCh38 chr1: 143,881,700-152,159,818 , GRCh37.p13 chr1|NW_003871055.3: 697,113-7,283,150 , PDIA3P1, 333 more genes
    nsv7044512inversion1nstd229human GRCh38 chr1: 151,026,124-151,042,147 , GRCh37.p13 chr1: 150,998,600-151,014,623 BNIPL, PRUNE1
    nsv7044458inversion1nstd229human GRCh38 chr1: 150,355,899-155,246,175 , GRCh37.p13 chr1: 150,440,214-155,215,966 LCE2C, MUC1, 254 more genes
    nsv7042502inversion1nstd229human GRCh38 chr1: 150,301,267-155,517,761 , GRCh37.p13 chr1: 150,440,214-155,487,552 LINGO4, CELF3, 268 more genes
    nsv6641933copy number variation1nstd229human GRCh38 chr1: 151,026,992-151,027,825 , GRCh37.p13 chr1: 150,999,468-151,000,301 PRUNE1
    nsv6641780copy number variation1nstd229human GRCh38 chr1: 151,026,183-151,056,469 , GRCh37.p13 chr1: 150,998,659-151,028,945 CDC42SE1, C1orf56, 2 more genes
    nsv6641777copy number variation1nstd229human GRCh38 chr1: 150,967,801-151,307,200 , GRCh37.p13 chr1: 150,940,277-151,279,676 MINDY1, TNFAIP8L2, 23 more genes
    nsv6641764copy number variation1nstd229human GRCh38 chr1: 150,761,787-151,277,656 , GRCh37.p13 chr1: 150,734,263-151,250,132 VPS72, RPS29P29, 30 more genes
    nsv6625395copy number variation1nstd224human GRCh37 chr1: 150,951,477-151,011,437 , GRCh38.p12 chr1: 150,979,001-151,038,961 ANXA9, MINDY1, 4 more genes
    nsv6550036inversion1nstd223human GRCh38 chr1: 151,020,876-151,022,360 , GRCh37.p13 chr1: 150,993,352-150,994,836 RNU6-884P, PRUNE1
    nsv6325299copy number variation1nstd223human GRCh38 chr1: 151,018,956-151,021,286 , GRCh37.p13 chr1: 150,991,432-150,993,762 PRUNE1, RNU6-884P
    nsv6321731copy number variation1nstd223human GRCh38 chr1: 151,033,026-151,033,337 , GRCh37.p13 chr1: 151,005,502-151,005,813 PRUNE1
    nsv6320256copy number variation1nstd223human GRCh38 chr1: 151,026,992-151,027,825 , GRCh37.p13 chr1: 150,999,468-151,000,301 PRUNE1
    nsv6318092copy number variation1nstd223human GRCh38 chr1: 151,020,201-151,023,900 , GRCh37.p13 chr1: 150,992,677-150,996,376 RNU6-884P, PRUNE1
    nsv6315606copy number variation1nstd223human GRCh38 chr1: 151,025,763-151,027,017 , GRCh37.p13 chr1: 150,998,239-150,999,493 PRUNE1
    nsv6310678copy number variation4nstd102humanUncertain significance GRCh37 chr1: 149,895,434-156,851,434 , GRCh38.p12 chr1: 149,923,542-156,881,642 PRPF3, KHDC4, 352 more genes
    nsv6300244copy number variation1nstd186human GRCh37 chr1: 151,002,030-151,006,099 , GRCh38.p12 chr1: 151,029,554-151,033,623 PRUNE1
    nsv6294010mobile element insertion1nstd186human GRCh37 chr1: 151,002,291-151,002,342 , GRCh38.p12 chr1: 151,029,815-151,029,866 PRUNE1
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