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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7141493insertion1nstd232human GRCh37.p13 chr1: 115,043,531-115,043,531 , GRCh38.p12 chr1: 114,500,909-114,500,909 TRIM33
    nsv7099225copy number variation1nstd231human GRCh38.p12 chr1: 111,381,594-114,553,029 , GRCh37 chr1: 111,924,216-115,095,650 ADORA3, RHOC, 74 more genes
    nsv7095740copy number variation1nstd102humanUncertain significance GRCh37 chr1: 113,456,513-116,311,162 , GRCh38.p12 chr1: 112,913,891-115,768,541 TRIM33, PHTF1, 55 more genes
    nsv7095696copy number variation1nstd102humanPathogenic GRCh37 chr1: 112,318,699-115,576,848 , GRCh38.p12 chr1: 111,776,077-115,034,227 AKR7A2P1, PTPN22, 69 more genes
    nsv7050397inversion1nstd229human GRCh38 chr1: 114,443,980-114,443,994 , GRCh37.p13 chr1: 114,986,602-114,986,616 TRIM33
    nsv7039033inversion1nstd229human GRCh38 chr1: 113,396,540-116,450,790 , GRCh37.p13 chr1: 113,939,162-116,993,412 ELOCP20, NHLH2, 60 more genes
    nsv6640400copy number variation1nstd229human GRCh38 chr1: 114,511,437-114,511,491 , GRCh37.p13 chr1: 115,054,058-115,054,112 TRIM33
    nsv6640399copy number variation1nstd229human GRCh38 chr1: 114,486,454-114,498,915 , GRCh37.p13 chr1: 115,029,076-115,041,537 TRIM33
    nsv6640398copy number variation1nstd229human GRCh38 chr1: 114,484,595-114,490,840 , GRCh37.p13 chr1: 115,027,217-115,033,462 TRIM33
    nsv6640372copy number variation1nstd229human GRCh38 chr1: 114,470,050-114,472,477 , GRCh37.p13 chr1: 115,012,672-115,015,099 EIF2S2P5, TRIM33
    nsv6640371copy number variation1nstd229human GRCh38 chr1: 114,448,258-114,451,549 , GRCh37.p13 chr1: 114,990,880-114,994,171 TRIM33
    nsv6640279copy number variation1nstd229human GRCh38 chr1: 114,419,552-114,420,291 , GRCh37.p13 chr1: 114,962,174-114,962,913 TRIM33
    nsv6640187copy number variation1nstd229human GRCh38 chr1: 114,435,567-114,439,672 , GRCh37.p13 chr1: 114,978,189-114,982,294 TRIM33
    nsv6636396copy number variation1nstd102humanUncertain significance GRCh37 chr1: 114,833,697-115,377,089 , GRCh38.p12 chr1: 114,291,075-114,834,468 NR1H5P, RN7SL432P, 13 more genes
    nsv6555350inversion1nstd223human GRCh38 chr1: 114,470,954-114,471,309 , GRCh37.p13 chr1: 115,013,576-115,013,931 TRIM33
    nsv6552536inversion1nstd223human GRCh38 chr1: 114,436,272-114,436,636 , GRCh37.p13 chr1: 114,978,894-114,979,258 TRIM33
    nsv6549317inversion1nstd223human GRCh38 chr1: 111,078,274-116,976,218 , GRCh37.p13 chr1: 111,620,896-117,518,840 RNU6-792P, TXNP3, 141 more genes
    nsv6545837inversion1nstd223human GRCh38 chr1: 114,474,064-114,474,332 , GRCh37.p13 chr1: 115,016,686-115,016,954 TRIM33
    nsv6541185inversion1nstd223human GRCh38 chr1: 114,436,261-114,436,746 , GRCh37.p13 chr1: 114,978,883-114,979,368 TRIM33
    nsv6539749inversion1nstd223human GRCh38 chr1: 114,436,167-114,436,764 , GRCh37.p13 chr1: 114,978,789-114,979,386 TRIM33
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