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Items: 1 to 20 of 247

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7074377inversion1nstd229human GRCh38 chr19: 41,965,396-49,981,454 , GRCh37.p13 chr19: 42,514,712-50,484,711 IGFL1, SYMPK, 400 more genes
    nsv7066709inversion1nstd229human GRCh38 chr19: 40,109,835-46,893,669 , GRCh37.p13 chr19: 40,615,742-47,396,926 LOC105372405, RNU6-611P, 305 more genes
    nsv7066137inversion1nstd229human GRCh38 chr19: 43,668,049-45,225,177 , GRCh37.p13 chr19: 44,172,201-45,728,435 LOC107985306, LYPD5, 67 more genes
    nsv7059316inversion1nstd229human GRCh38 chr19: 43,396,877-48,200,638 , GRCh37.p13 chr19: 43,901,029-48,703,895 GEMIN7, ZNF229, 212 more genes
    nsv7017281copy number variation1nstd229human GRCh38 chr19: 44,845,201-44,857,900 , GRCh37.p13 chr19: 45,348,458-45,361,157 NECTIN2
    nsv7017044copy number variation1nstd229human GRCh38 chr19: 44,852,853-44,862,899 , GRCh37.p13 chr19: 45,356,110-45,366,156 NECTIN2
    nsv7015916copy number variation1nstd229human GRCh38 chr19: 44,838,371-44,844,969 , GRCh37.p13 chr19: 45,341,628-45,348,226 NECTIN2
    nsv7008156copy number variation1nstd229human GRCh38 chr19: 36,851,242-46,031,790 , GRCh37.p13 chr19: 37,342,144-46,535,048 LOC105372390, LOC107985291, 396 more genes
    nsv7004486copy number variation1nstd229human GRCh38 chr19: 44,793,721-44,893,913 , GRCh37.p13 chr19: 45,296,978-45,397,170 CBLC, TOMM40, 2 more genes
    nsv6596646inversion1nstd223human GRCh38 chr19: 44,885,124-44,885,910 , GRCh37.p13 chr19: 45,388,381-45,389,167 NECTIN2
    nsv6527454copy number variation1nstd223human GRCh38 chr19: 44,855,203-44,862,263 , GRCh37.p13 chr19: 45,358,460-45,365,520 NECTIN2
    nsv6524231copy number variation1nstd223human GRCh38 chr19: 44,855,324-44,856,200 , GRCh37.p13 chr19: 45,358,581-45,359,457 NECTIN2
    nsv6523815copy number variation1nstd223human GRCh38 chr19: 44,276,620-45,370,613 , GRCh37.p13 chr19: 44,780,773-45,873,871 APOE, CEACAM16, 48 more genes
    nsv6523800copy number variation1nstd223human GRCh38 chr19: 44,866,228-44,869,335 , GRCh37.p13 chr19: 45,369,485-45,372,592 NECTIN2
    nsv6314081copy number variation1nstd102humanUncertain significance GRCh37 chr19: 45,074,342-46,133,841 , GRCh38.p12 chr19: 44,571,096-45,630,583 EXOC3L2, APOE, 50 more genes
    nsv6212948copy number variation1nstd214human GRCh38 chr19: 44,845,163-44,845,250 , GRCh37.p13 chr19: 45,348,420-45,348,507 NECTIN2
    nsv6133704copy number variation1nstd213human GRCh37 chr19: 45,030,000-55,230,001 , GRCh38.p12 chr19: 44,525,967-54,071,460 AP2A1, APOC1, 582 more genes
    nsv6133703copy number variation1nstd213human GRCh37 chr19: 41,220,000-49,640,001 , GRCh38.p12 chr19: 40,714,095-49,136,744 , APOC1, 402 more genes
    nsv6133474copy number variation1nstd213human GRCh37 chr19: 42,350,000-49,650,001 , GRCh38.p12 chr19: 41,845,937-49,146,744 , APOC1, 343 more genes
    nsv5883567copy number variation1nstd209human GRCh38 chr19: 44,866,494-44,867,493 , GRCh37.p13 chr19: 45,369,751-45,370,750 NECTIN2
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