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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
    nsv7095726copy number variation1nstd102humanPathogenic GRCh37 chr19: 6,361,586-8,212,364 , GRCh38.p12 chr19: 6,361,575-8,147,480 SLC25A23, LYPLA2P2, 77 more genes
    nsv7095676copy number variation1nstd102humanUncertain significance GRCh37 chr19: 7,586,521-8,670,595 , GRCh38.p12 chr19: 7,521,635-8,605,710 LRRC8E, ZNF414, 53 more genes
    nsv7070187inversion1nstd229human GRCh38 chr19: 6,518,823-8,315,881 , GRCh37.p13 chr19: 6,518,834-8,380,765 , ZNF557, 69 more genes
    nsv7066716inversion1nstd229human GRCh38 chr19: 6,518,017-8,344,162 , GRCh37.p13 chr19: 6,518,028-8,409,046 , STXBP2, 71 more genes
    nsv7062847inversion1nstd229human GRCh38 chr19: 7,473,530-8,349,302 , GRCh37.p13 chr19: 7,538,416-8,414,186 CERS4, LYPLA2P2, 47 more genes
    nsv7013524copy number variation1nstd229human GRCh38 chr19: 7,623,595-7,921,993 , GRCh37.p13 chr19: 7,688,481-7,986,878 STXBP2, LOC100129391, 24 more genes
    nsv7012889copy number variation1nstd229human GRCh38 chr19: 7,616,098-7,695,916 , GRCh37.p13 chr19: 7,680,984-7,760,802 MCEMP1, RETN, 9 more genes
    nsv7011964copy number variation1nstd229human GRCh38 chr19: 7,354,369-9,019,195 , GRCh37.p13 chr19: 7,419,271-9,129,871 , MCOLN1, 66 more genes
    nsv7011121copy number variation1nstd229human GRCh38 chr19: 7,159,006-9,938,147 , GRCh37.p13 chr19: 7,159,017-10,048,823 , OR7G1, 117 more genes
    nsv7009810copy number variation1nstd229human GRCh38 chr19: 7,661,801-7,669,200 , GRCh37.p13 chr19: 7,726,687-7,734,086 RETN, RPS27AP19
    nsv7008722copy number variation1nstd229human GRCh38 chr19: 7,653,504-7,737,408 , GRCh37.p13 chr19: 7,718,390-7,802,294 TRAPPC5, FCER2, 5 more genes
    nsv6999416copy number variation1nstd229human GRCh38 chr19: 7,659,138-7,677,578 , GRCh37.p13 chr19: 7,724,024-7,742,464 RPS27AP19, RETN, 1 more genes
    nsv6625331copy number variation1nstd224human GRCh37 chr19: 7,663,768-7,881,030 , GRCh38.p12 chr19: 7,598,882-7,816,144 FCER2, STXBP2, 18 more genes
    nsv6524814copy number variation1nstd223human GRCh38 chr19: 7,666,623-7,667,773 , GRCh37.p13 chr19: 7,731,509-7,732,659 RETN, RPS27AP19
    nsv6516661copy number variation1nstd223human GRCh38 chr19: 7,659,061-7,686,708 , GRCh37.p13 chr19: 7,723,947-7,751,594 TRAPPC5, RETN, 2 more genes
    nsv6133698copy number variation1nstd213human GRCh37 chr19: 2,900,000-11,490,001 , GRCh38.p12 chr19: 2,900,002-11,379,325 , TLE5, 341 more genes
    nsv6133479copy number variation1nstd213human GRCh37 chr19: 7,400,000-13,280,001 , GRCh38.p12 chr19: 7,335,095-13,169,187 , ACP5, 299 more genes
    nsv6045597copy number variation1nstd212human GRCh38 chr19: 7,667,296-7,667,740 , GRCh37.p13 chr19: 7,732,182-7,732,626 RETN
    nsv5327606copy number variation1nstd204human GRCh37.p13 chr19: 7,731,285-7,786,574 , GRCh38.p13 chr19: 7,666,399-7,721,688 FCER2, RETN, 4 more genes
    nsv5294004copy number variation1nstd204human GRCh38.p13 chr19: 7,666,644-7,695,815 , GRCh37.p13 chr19: 7,731,530-7,760,701 RPS27AP19, FCER2, 3 more genes
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