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Items: 1 to 20 of 395

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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
    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
    nsv7067199inversion1nstd229human GRCh38 chr14: 103,669,994-103,670,083 , GRCh37.p13 chr14: 104,136,331-104,136,420 KLC1
    nsv7062190inversion1nstd229human GRCh38 chr14: 103,555,287-104,539,425 , GRCh37.p13 chr14: 104,021,624-104,966,919 RNU4-68P, MIR203B, 21 more genes
    nsv6977817copy number variation1nstd229human GRCh38 chr14: 103,673,601-103,934,800 , GRCh37.p13 chr14: 104,139,938-104,401,137 ZFYVE21, XRCC3, 7 more genes
    nsv6977174copy number variation1nstd229human GRCh38 chr14: 103,696,256-103,698,719 , GRCh37.p13 chr14: 104,162,593-104,165,056 XRCC3, KLC1
    nsv6976973copy number variation1nstd229human GRCh38 chr14: 103,699,881-103,736,493 , GRCh37.p13 chr14: 104,166,218-104,202,830 KLC1, PPP1R13B, 3 more genes
    nsv6973109copy number variation1nstd229human GRCh38 chr14: 103,697,861-103,697,892 , GRCh37.p13 chr14: 104,164,198-104,164,229 XRCC3, KLC1
    nsv6973016copy number variation1nstd229human GRCh38 chr14: 103,627,333-103,627,369 , GRCh37.p13 chr14: 104,093,670-104,093,706 KLC1, LOC105370688
    nsv6972210copy number variation1nstd229human GRCh38 chr14: 103,635,201-103,649,200 , GRCh37.p13 chr14: 104,101,538-104,115,537 KLC1
    nsv6972118copy number variation1nstd229human GRCh38 chr14: 103,664,288-103,667,473 , GRCh37.p13 chr14: 104,130,625-104,133,810 KLC1
    nsv6971508copy number variation1nstd229human GRCh38 chr14: 103,677,857-103,679,157 , GRCh37.p13 chr14: 104,144,194-104,145,494 KLC1
    nsv6967048copy number variation1nstd229human GRCh38 chr14: 103,461,701-103,827,300 , GRCh37.p13 chr14: 103,928,038-104,293,637 COA8, XRCC3, 12 more genes
    nsv6966907copy number variation1nstd229human GRCh38 chr14: 103,341,601-103,757,500 , GRCh37.p13 chr14: 103,807,938-104,223,837 TRMT61A, RNU7-160P, 16 more genes
    nsv6964827copy number variation1nstd229human GRCh38 chr14: 103,648,957-103,693,780 , GRCh37.p13 chr14: 104,115,294-104,160,117 KLC1
    nsv6962902copy number variation1nstd229human GRCh38 chr14: 103,686,971-103,735,785 , GRCh37.p13 chr14: 104,153,308-104,202,122 ZFYVE21, XRCC3, 3 more genes
    nsv6962231copy number variation1nstd229human GRCh38 chr14: 103,556,136-103,744,354 , GRCh37.p13 chr14: 104,022,473-104,210,691 COA8, LOC105370688, 7 more genes
    nsv6637825copy number variation1nstd102humanPathogenic GRCh37 chr14: 84,537,502-107,285,437 , GRCh38.p12 chr14: 84,071,158-106,877,229 CHGA, SNORD114-26, 676 more genes
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