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Items: 1 to 20 of 185

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5956548insertion1nstd209human GRCh38 chr3: 113,015,584-113,015,584 , GRCh37.p13 chr3: 112,734,431-112,734,431 NEPRO
    nsv5691431mobile element insertion2nstd211human GRCh38 chr3: 113,015,598-113,015,598 , GRCh37.p13 chr3: 112,734,445-112,734,445 NEPRO
    nsv5689321mobile element insertion1nstd211human GRCh38 chr3: 113,013,648-113,013,648 , GRCh37.p13 chr3: 112,732,495-112,732,495 NEPRO
    nsv5613822insertion1nstd207human GRCh38 chr3: 113,015,584-113,015,584 , GRCh37.p13 chr3: 112,734,431-112,734,431 NEPRO
    nsv5412854mobile element insertion1nstd206human GRCh38 chr3: 113,015,598-113,015,649 , GRCh37.p13 chr3: 112,734,445-112,734,496 NEPRO
    nsv5098485mobile element insertion1nstd203human GRCh38 chr3: 113,015,591-113,015,598 , GRCh37.p13 chr3: 112,734,438-112,734,445 NEPRO
    nsv5084547mobile element insertion1nstd203human GRCh38 chr3: 113,015,584-113,015,598 , GRCh37.p13 chr3: 112,734,431-112,734,445 NEPRO
    nsv5036857inversion1nstd200human GRCh38 chr3: 97,392,267-146,717,859 , GRCh37.p13 chr3: 97,111,111-146,435,646 , FBRSL1P1, 801 more genes
    nsv5031637inversion1nstd200human GRCh38 chr3: 112,181,184-125,673,487 , GRCh37.p13 chr3: 111,900,031-125,392,331 , ARHGAP31, 218 more genes
    nsv4914623copy number variation1nstd200human GRCh38 chr3: 109,310,668-113,023,370 , GRCh37.p13 chr3: 109,029,515-112,742,217 , CD200R1, 55 more genes
    nsv4750742insertion1nstd199human GRCh37 chr3: 112,734,444-112,734,444 , GRCh38.p12 chr3: 113,015,597-113,015,597 NEPRO
    nsv4728380copy number variation1nstd102humanPathogenic GRCh37 chr3: 112,135,341-115,509,260 , GRCh38.p12 chr3: 112,416,494-115,790,413 SLC35A5, EIF4E2P2, 51 more genes
    nsv4726219insertion1nstd186human GRCh37 chr3: 112,734,431-112,734,431 , GRCh38.p12 chr3: 113,015,584-113,015,584 NEPRO
    nsv4691911mobile element insertion1nstd186human GRCh37 chr3: 112,734,445-112,734,445 , GRCh38.p12 chr3: 113,015,598-113,015,598 NEPRO
    nsv4595961copy number variation1nstd183human GRCh37 chr3: 111,977,032-113,013,191 , GRCh38.p12 chr3: 112,258,185-113,294,344 , NEPRO-AS1, 22 more genes
    nsv4578248copy number variation1nstd102humanPathogenic GRCh37 chr3: 112,183,943-115,492,949 , GRCh38.p12 chr3: 112,465,096-115,774,102 ZBTB20, ZBTB20-AS1, 51 more genes
    nsv4543394insertion1nstd166human GRCh37.p13 chr3: 112,734,431-112,734,431 , GRCh38.p12 chr3: 113,015,584-113,015,584 NEPRO
    nsv4452572copy number variation2nstd102humanUncertain significance GRCh37 chr3: 111,929,014-112,773,945 , GRCh38.p12 chr3: 112,210,167-113,055,098 MIR9900, CD200, 16 more genes
    nsv4317801inversion1nstd166human GRCh37.p13 chr3: 106,160,269-123,476,086 , GRCh38.p12 chr3: 106,441,422-123,757,239 , ADPRH, 270 more genes
    nsv4077316copy number variation1nstd166human GRCh37.p13 chr3: 112,734,945-112,735,364 , GRCh38.p12 chr3: 113,016,098-113,016,517 NEPRO
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