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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099226copy number variation1nstd231human GRCh38.p12 chr1: 115,063,638-119,984,872 , GRCh37 chr1: 115,606,259-120,527,495 ATP1A1, CASQ2, 103 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
    nsv7054531inversion1nstd229human GRCh38 chr1: 115,607,811-115,998,820 , GRCh37.p13 chr1: 116,150,432-116,541,441 SLC22A15, NHLH2, 6 more genes
    nsv7039033inversion1nstd229human GRCh38 chr1: 113,396,540-116,450,790 , GRCh37.p13 chr1: 113,939,162-116,993,412 ELOCP20, NHLH2, 60 more genes
    nsv6640631copy number variation1nstd229human GRCh38 chr1: 115,697,913-115,697,947 , GRCh37.p13 chr1: 116,240,534-116,240,568 VANGL1
    nsv6640629copy number variation1nstd229human GRCh38 chr1: 115,650,905-115,653,992 , GRCh37.p13 chr1: 116,193,526-116,196,613 VANGL1
    nsv6640541copy number variation1nstd229human GRCh38 chr1: 115,591,942-115,821,742 , GRCh37.p13 chr1: 116,134,563-116,364,363 RN7SL420P, CASQ2, 1 more genes
    nsv6640447copy number variation1nstd229human GRCh38 chr1: 115,686,865-115,690,223 , GRCh37.p13 chr1: 116,229,486-116,232,844 VANGL1
    nsv6640229copy number variation1nstd229human GRCh38 chr1: 115,685,401-115,690,200 , GRCh37.p13 chr1: 116,228,022-116,232,821 VANGL1
    nsv6640228copy number variation1nstd229human GRCh38 chr1: 115,665,812-115,668,217 , GRCh37.p13 chr1: 116,208,433-116,210,838 VANGL1
    nsv6640227copy number variation1nstd229human GRCh38 chr1: 115,653,601-115,739,300 , GRCh37.p13 chr1: 116,196,222-116,281,921 VANGL1, CASQ2
    nsv6625547copy number variation1nstd224human GRCh37 chr1: 116,239,368-116,286,983 , GRCh38.p12 chr1: 115,696,747-115,744,362 CASQ2, VANGL1
    nsv6549317inversion1nstd223human GRCh38 chr1: 111,078,274-116,976,218 , GRCh37.p13 chr1: 111,620,896-117,518,840 RNU6-792P, TXNP3, 141 more genes
    nsv6331169copy number variation1nstd223human GRCh38 chr1: 115,691,217-115,745,168 , GRCh37.p13 chr1: 116,233,838-116,287,789 CASQ2, VANGL1
    nsv6317133copy number variation1nstd223human GRCh38 chr1: 115,685,001-115,690,200 , GRCh37.p13 chr1: 116,227,622-116,232,821 VANGL1
    nsv6313671copy number variation1nstd102humanPathogenic GRCh37 chr1: 111,647,582-121,343,783 , GRCh38.p12 chr1: 111,104,960-121,601,985 GAPDHP23, RNA5SP56, 243 more genes
    nsv6133549copy number variation1nstd213human GRCh37 chr1: 116,100,000-117,130,001 , GRCh38.p12 chr1: 115,557,379-116,587,379 HNRNPA1P43, NAP1L4P1, 26 more genes
    nsv5980861copy number variation1nstd212human GRCh38 chr1: 115,653,242-115,653,322 , GRCh37.p13 chr1: 116,195,863-116,195,943 VANGL1
    nsv5980778copy number variation1nstd212human GRCh38 chr1: 115,686,862-115,690,219 , GRCh37.p13 chr1: 116,229,483-116,232,840 VANGL1
    nsv5879067copy number variation1nstd209human GRCh38 chr1: 115,686,862-115,690,218 , GRCh37.p13 chr1: 116,229,483-116,232,839 VANGL1
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