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Items: 1 to 20 of 146

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095478copy number variation1nstd102humanUncertain significance GRCh37 chr19: 33,167,170-36,643,309 , GRCh38.p12 chr19: 32,676,264-36,152,407 NFKBID, LRP3, 141 more genes
    nsv7074671inversion1nstd229human GRCh38 chr19: 33,126,299-36,006,645 , GRCh37.p13 chr19: 33,617,205-36,497,547 , ZNF30, 120 more genes
    nsv7074279inversion1nstd229human GRCh38 chr19: 33,135,428-36,017,833 , GRCh37.p13 chr19: 33,626,334-36,508,735 , PSENEN, 122 more genes
    nsv7072782inversion1nstd229human GRCh38 chr19: 34,537,710-34,749,334 , GRCh37.p13 chr19: 35,028,615-35,240,239 SCGB2B2, SCGB2B1P, 9 more genes
    nsv7060096inversion1nstd229human GRCh38 chr19: 34,537,753-34,746,067 , GRCh37.p13 chr19: 35,028,658-35,236,972 SCGB1B2P, ZNF302, 9 more genes
    nsv7016351copy number variation1nstd229human GRCh38 chr19: 34,742,223-34,742,322 , GRCh37.p13 chr19: 35,233,128-35,233,227 ZNF181
    nsv7005713copy number variation1nstd229human GRCh38 chr19: 33,458,650-39,721,746 , GRCh37.p13 chr19: 33,949,556-40,212,386 , TYROBP, 259 more genes
    nsv7005257copy number variation1nstd229human GRCh38 chr19: 34,737,492-34,737,833 , GRCh37.p13 chr19: 35,228,397-35,228,738 ZNF181
    nsv7001541copy number variation1nstd229human GRCh38 chr19: 34,745,227-34,745,546 , GRCh37.p13 chr19: 35,236,132-35,236,451 ZNF181
    nsv6598572inversion1nstd223human GRCh38 chr19: 34,537,710-34,749,334 , GRCh37.p13 chr19: 35,028,615-35,240,239 ZNF807P, LOC100130632, 9 more genes
    nsv6314074copy number variation1nstd102humanUncertain significance GRCh37 chr19: 32,827,535-35,263,640 , GRCh38.p12 chr19: 32,336,629-34,772,735 LOC100130632, CEP89, 59 more genes
    nsv6307118copy number variation1nstd186human GRCh37 chr19: 35,235,779-35,240,905 , GRCh38.p12 chr19: 34,744,874-34,750,000 ZNF181
    nsv6290300copy number variation1nstd102humanPathogenic GRCh37 chr19: 19,546,923-41,313,229 , GRCh38.p12 chr19: 19,436,114-40,807,324 ZNF420, LOC105372330, 574 more genes
    nsv6145793copy number variation1nstd206human GRCh38 chr19: 34,744,874-34,750,000 , GRCh37.p13 chr19: 35,235,779-35,240,905 ZNF181
    nsv6133523copy number variation1nstd213human GRCh37 chr19: 34,000,000-42,200,001 , GRCh38.p12 chr19: 33,509,094-41,696,083 , ACTN4, 345 more genes
    nsv6104002inversion1nstd212human GRCh38 chr19: 34,537,754-34,750,577 , GRCh37.p13 chr19: 35,028,659-35,241,482 ZNF302, SCGB2B2, 9 more genes
    nsv5975015inversion1nstd209human GRCh38 chr19: 34,537,657-34,749,386 , GRCh37.p13 chr19: 35,028,562-35,240,291 ZNF302, SCGB2B2, 9 more genes
    nsv5941922copy number variation1nstd209human GRCh38 chr19: 34,742,740-34,742,838 , GRCh37.p13 chr19: 35,233,645-35,233,743 ZNF181
    nsv5873546copy number variation1nstd209human GRCh38 chr19: 34,746,100-34,748,641 , GRCh37.p13 chr19: 35,237,005-35,239,546 ZNF181
    nsv5701272mobile element insertion1nstd211human GRCh38 chr19: 34,742,522-34,742,522 , GRCh37.p13 chr19: 35,233,427-35,233,427 ZNF181
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