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Items: 1 to 20 of 104

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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
    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
    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
    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
    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
    nsv6278950copy number variation1nstd214human GRCh38 chr19: 45,073,531-45,073,602 , GRCh37.p13 chr19: 45,576,789-45,576,860 ZNF296
    nsv6146670copy number variation1nstd206human GRCh38 chr19: 45,062,572-45,072,879 , GRCh37.p13 chr19: 45,565,830-45,576,137 CLASRP, ZNF296
    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
    nsv5933499copy number variation1nstd209human GRCh38 chr19: 45,073,531-45,073,602 , GRCh37.p13 chr19: 45,576,789-45,576,860 ZNF296
    nsv5929013copy number variation1nstd209human GRCh38 chr19: 45,073,984-45,074,322 , GRCh37.p13 chr19: 45,577,242-45,577,580 ZNF296, GEMIN7
    nsv5521357copy number variation1nstd206human GRCh38 chr19: 45,073,532-45,073,603 , GRCh37.p13 chr19: 45,576,790-45,576,861 ZNF296
    nsv5020665copy number variation1nstd200human GRCh38 chr19: 45,075,182-45,075,296 , GRCh37.p13 chr19: 45,578,440-45,578,554 ZNF296, GEMIN7
    nsv4676357copy number variation1nstd102humanPathogenic GRCh37 chr19: 44,738,088-53,621,561 , GRCh38.p12 chr19: 44,233,935-53,118,308 MIR4324, KLK9, 485 more genes
    nsv4676350copy number variation1nstd102humanUncertain significance GRCh37 chr19: 45,531,056-48,174,177 , GRCh38.p12 chr19: 45,027,798-47,670,920 NKPD1, IGFL1, 112 more genes
    nsv4631923copy number variation1nstd183human GRCh37 chr19: 45,525,537-45,768,917 , GRCh38.p12 chr19: 45,022,279-45,265,659 BLOC1S3, CLASRP, 13 more genes
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