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Items: 1 to 20 of 173

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7144185insertion1nstd232human GRCh37.p13 chr19: 7,708,899-7,708,899 , GRCh38.p12 chr19: 7,644,013-7,644,013 STXBP2
    nsv7095728copy number variation1nstd102humanLikely pathogenic GRCh37 chr19: 7,703,306-7,707,110 , GRCh38.p12 chr19: 7,638,420-7,642,224 STXBP2
    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
    nsv7067646inversion1nstd229human GRCh38 chr19: 2,282,380-7,636,598 , GRCh37.p13 chr19: 2,282,379-7,701,484 , UHRF1, 192 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
    nsv7017151copy number variation1nstd229human GRCh38 chr19: 7,307,424-7,664,280 , GRCh37.p13 chr19: 7,396,129-7,729,166 , PNPLA6, 13 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
    nsv7012594copy number variation1nstd229human GRCh38 chr19: 7,648,067-7,651,288 , GRCh37.p13 chr19: 7,712,953-7,716,174 STXBP2
    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
    nsv7003831copy number variation1nstd229human GRCh38 chr19: 7,617,680-7,657,473 , GRCh37.p13 chr19: 7,682,566-7,722,359 CAMSAP3, PCP2, 4 more genes
    nsv6999645copy number variation1nstd229human GRCh38 chr19: 7,639,321-7,641,546 , GRCh37.p13 chr19: 7,704,207-7,706,432 STXBP2
    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
    nsv6597296inversion1nstd223human GRCh38 chr19: 2,282,380-7,636,598 , GRCh37.p13 chr19: 2,282,379-7,701,484 , ALKBH7, 192 more genes
    nsv6520929copy number variation1nstd223human GRCh38 chr19: 7,617,680-7,657,473 , GRCh37.p13 chr19: 7,682,566-7,722,359 MIR6792, STXBP2, 4 more genes
    nsv6520175copy number variation1nstd223human GRCh38 chr19: 7,643,807-7,643,978 , GRCh37.p13 chr19: 7,708,693-7,708,864 STXBP2
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