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Items: 1 to 20 of 150

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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
    nsv7074281inversion1nstd229human GRCh38 chr19: 45,085,820-45,086,982 , GRCh37.p13 chr19: 45,589,078-45,590,240 GEMIN7-AS1, GEMIN7
    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
    nsv7012524copy number variation1nstd229human GRCh38 chr19: 45,087,140-45,092,489 , GRCh37.p13 chr19: 45,590,398-45,595,747 PPP1R37, GEMIN7-AS1, 1 more genes
    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
    nsv6998432copy number variation1nstd229human GRCh38 chr19: 45,078,722-45,080,892 , GRCh37.p13 chr19: 45,581,980-45,584,150 GEMIN7
    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
    nsv6522111copy number variation1nstd223human GRCh38 chr19: 45,078,388-45,085,034 , GRCh37.p13 chr19: 45,581,646-45,588,292 GEMIN7-AS1, GEMIN7
    nsv6519752copy number variation1nstd223human GRCh38 chr19: 45,086,901-45,088,000 , GRCh37.p13 chr19: 45,590,159-45,591,258 GEMIN7, GEMIN7-AS1
    nsv6517662copy number variation1nstd223human GRCh38 chr19: 45,051,352-45,087,289 , GRCh37.p13 chr19: 45,554,610-45,590,547 ZNF296, CLASRP, 2 more genes
    nsv6517532copy number variation1nstd223human GRCh38 chr19: 45,087,501-45,088,200 , GRCh37.p13 chr19: 45,590,759-45,591,458 GEMIN7, GEMIN7-AS1
    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
    nsv6147401sequence alteration1nstd206human GRCh38 chr19: 45,084,978-45,085,123 , GRCh37.p13 chr19: 45,588,236-45,588,381 GEMIN7, GEMIN7-AS1
    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
    nsv6103268inversion1nstd212human GRCh38 chr19: 45,080,087-46,509,008 , GRCh37.p13 chr19: 45,583,345-47,012,265 , CKM, 72 more genes
    nsv5937937copy number variation1nstd209human GRCh38 chr19: 45,087,343-45,088,144 , GRCh37.p13 chr19: 45,590,601-45,591,402 GEMIN7-AS1, GEMIN7
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