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Items: 1 to 20 of 193

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5894142copy number variation1nstd209human GRCh38 chr3: 112,921,012-112,921,214 , GRCh37.p13 chr3: 112,639,859-112,640,061 CD200R1
    nsv5610023insertion1nstd207human GRCh38 chr3: 112,926,344-112,926,344 , GRCh37.p13 chr3: 112,645,191-112,645,191 CD200R1
    nsv5441403copy number variation1nstd206human GRCh38 chr3: 112,896,585-112,926,235 , GRCh37.p13 chr3: 112,615,432-112,645,082 CD200R1
    nsv5441161copy number variation1nstd206human GRCh38 chr3: 112,915,307-112,920,016 , GRCh37.p13 chr3: 112,634,154-112,638,863 CD200R1
    nsv5237391copy number variation1nstd204human GRCh38.p13 chr3: 112,938,501-112,945,100 , GRCh37.p13 chr3: 112,657,348-112,663,947 CD200R1
    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
    nsv4919580copy number variation1nstd200human GRCh38 chr3: 112,945,909-112,953,095 , GRCh37.p13 chr3: 112,664,756-112,671,942 CD200R1
    nsv4919579copy number variation1nstd200human GRCh38 chr3: 112,945,238-112,949,031 , GRCh37.p13 chr3: 112,664,085-112,667,878 CD200R1
    nsv4919578copy number variation1nstd200human GRCh38 chr3: 112,935,043-112,940,395 , GRCh37.p13 chr3: 112,653,890-112,659,242 CD200R1
    nsv4914623copy number variation1nstd200human GRCh38 chr3: 109,310,668-113,023,370 , GRCh37.p13 chr3: 109,029,515-112,742,217 , CD200R1, 55 more genes
    nsv4806791copy number variation1nstd200human GRCh37 chr3: 112,664,756-112,671,942 , GRCh38.p12 chr3: 112,945,909-112,953,095 CD200R1
    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
    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
    nsv4467930mobile element insertion1nstd166human GRCh37.p13 chr3: 112,670,173-112,670,173 , GRCh38.p12 chr3: 112,951,326-112,951,326 CD200R1
    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
    nsv4092082copy number variation1nstd166human GRCh37.p13 chr3: 112,664,085-112,667,879 , GRCh38.p12 chr3: 112,945,238-112,949,032 CD200R1
    nsv4072933copy number variation1nstd166human GRCh37.p13 chr3: 112,634,000-112,639,000 , GRCh38.p12 chr3: 112,915,153-112,920,153 CD200R1
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