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Items: 1 to 20 of 541

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148227copy number variation1nstd102humanPathogenic GRCh38 chr14: 102,263,440-106,874,929 , GRCh37.p13 chr14: 102,729,777-107,283,138 TNFAIP2, IGHV4-30-2, 306 more genes
    nsv7143714insertion1nstd232human GRCh37.p13 chr14: 104,698,229-104,698,229 , GRCh38.p12 chr14: 104,231,892-104,231,892 LINC02691
    nsv7137201copy number variation1nstd102humanPathogenic GRCh37 chr14: 103,636,647-107,285,437 , GRCh38.p12 chr14: 103,170,310-106,877,229 IGHD, IGH, 281 more genes
    nsv7094241copy number variation1nstd102humanUncertain significance GRCh37 chr14: 102,442,029-105,861,009 , GRCh38.p12 chr14: 101,975,692-105,394,672 LOC107984670, MARK3, 101 more genes
    nsv7094007copy number variation1nstd102humanUncertain significance GRCh37 chr14: 102,228,231-105,861,009 , GRCh38.p12 chr14: 101,761,894-105,394,672 CLBA1, BAG5, 105 more genes
    nsv7062190inversion1nstd229human GRCh38 chr14: 103,555,287-104,539,425 , GRCh37.p13 chr14: 104,021,624-104,966,919 RNU4-68P, MIR203B, 21 more genes
    nsv6978086copy number variation1nstd229human GRCh38 chr14: 104,235,455-104,235,519 , GRCh37.p13 chr14: 104,701,792-104,701,856 LINC02691
    nsv6978051copy number variation1nstd229human GRCh38 chr14: 104,255,851-104,256,036 , GRCh37.p13 chr14: 104,722,188-104,722,373 LINC02691
    nsv6977473copy number variation1nstd229human GRCh38 chr14: 104,219,243-104,322,400 , GRCh37.p13 chr14: 104,685,580-104,788,737 LINC02691
    nsv6975755copy number variation1nstd229human GRCh38 chr14: 104,223,610-104,232,947 , GRCh37.p13 chr14: 104,689,947-104,699,284 LINC02691
    nsv6975148copy number variation1nstd229human GRCh38 chr14: 104,284,846-104,287,440 , GRCh37.p13 chr14: 104,751,183-104,753,777 LINC02691
    nsv6972591copy number variation1nstd229human GRCh38 chr14: 104,236,235-104,244,614 , GRCh37.p13 chr14: 104,702,572-104,710,951 LINC02691
    nsv6971436copy number variation1nstd229human GRCh38 chr14: 104,264,186-104,271,265 , GRCh37.p13 chr14: 104,730,523-104,737,602 LINC02691
    nsv6970334copy number variation1nstd229human GRCh38 chr14: 104,281,171-104,309,100 , GRCh37.p13 chr14: 104,747,508-104,775,437 LINC02691
    nsv6969742copy number variation1nstd229human GRCh38 chr14: 104,244,212-104,253,706 , GRCh37.p13 chr14: 104,710,549-104,720,043 LINC02691
    nsv6969688copy number variation1nstd229human GRCh38 chr14: 104,057,242-104,269,659 , GRCh37.p13 chr14: 104,523,579-104,735,996 ASPG, MIR203A, 4 more genes
    nsv6967906copy number variation1nstd229human GRCh38 chr14: 104,058,547-104,336,906 , GRCh37.p13 chr14: 104,524,884-104,803,243 KIF26A-DT, MIR203B, 4 more genes
    nsv6967734copy number variation1nstd229human GRCh38 chr14: 104,196,551-104,238,228 , GRCh37.p13 chr14: 104,662,888-104,704,565 LINC02691
    nsv6965381copy number variation1nstd229human GRCh38 chr14: 104,286,551-104,290,484 , GRCh37.p13 chr14: 104,752,888-104,756,821 LINC02691
    nsv6964705copy number variation1nstd229human GRCh38 chr14: 104,281,300-104,281,444 , GRCh37.p13 chr14: 104,747,637-104,747,781 LINC02691
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