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Items: 1 to 20 of 313

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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
    nsv7094482copy number variation1nstd102humanUncertain significance GRCh37 chr14: 105,167,703-105,861,009 , GRCh38.p12 chr14: 104,701,366-105,394,672 AHNAK2, PLD4, 24 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
    nsv7071433inversion1nstd229human GRCh38 chr14: 104,657,007-104,731,085 , GRCh37.p13 chr14: 105,123,344-105,197,422 INF2, ADSS1, 2 more genes
    nsv6974945copy number variation1nstd229human GRCh38 chr14: 104,709,301-104,729,300 , GRCh37.p13 chr14: 105,175,638-105,195,637 INF2, ADSS1
    nsv6972195copy number variation1nstd229human GRCh38 chr14: 104,658,559-104,755,469 , GRCh37.p13 chr14: 105,124,896-105,221,806 INF2, ADSS1, 5 more genes
    nsv6968348copy number variation1nstd229human GRCh38 chr14: 104,726,201-104,732,600 , GRCh37.p13 chr14: 105,192,538-105,198,937 ADSS1
    nsv6965183copy number variation1nstd229human GRCh38 chr14: 104,735,501-104,741,600 , GRCh37.p13 chr14: 105,201,838-105,207,937 ADSS1, LOC107984670
    nsv6961308copy number variation1nstd229human GRCh38 chr14: 104,494,808-104,931,788 , GRCh37.p13 chr14: 104,961,145-105,398,125 LINC02280, SIVA1, 16 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
    nsv6505209copy number variation1nstd223human GRCh38 chr14: 104,735,541-104,741,606 , GRCh37.p13 chr14: 105,201,878-105,207,943 ADSS1, LOC107984670
    nsv6315524copy number variation1nstd102humanPathogenic GRCh37 chr14: 37,671,058-106,985,955 , GRCh38.p12 chr14: 37,201,853-106,530,013 PAPOLA-DT, LOC105378180, 1338 more genes
    nsv6314860copy number variation1nstd102humanUncertain significance GRCh37 chr14: 103,336,539-105,861,009 , GRCh38.p12 chr14: 102,870,202-105,394,672 PLD4, AHNAK2, 80 more genes
    nsv6314796copy number variation1nstd102humanPathogenic GRCh37 chr14: 105,204,693-105,207,600 , GRCh38.p12 chr14: 104,738,356-104,741,263 ADSS1, LOC107984670
    nsv6314048copy number variation1nstd102humanPathogenic GRCh37 chr14: 101,732,158-107,285,437 , GRCh38.p12 chr14: 101,265,821-106,877,229 IGHD4-23, XRCC3, 329 more genes
    nsv6309688copy number variation1nstd102humanUncertain significance GRCh37 chr14: 105,167,703-105,213,340 , GRCh38.p12 chr14: 104,701,366-104,747,003 ADSS1, LOC107987209, 2 more genes
    nsv6309344copy number variation1nstd102humanUncertain significance GRCh37 chr14: 102,229,222-105,861,009 , GRCh38.p12 chr14: 101,762,885-105,394,672 LOC107984648, RN7SL634P, 105 more genes
    nsv6291499copy number variation1nstd102humanPathogenic GRCh37 chr14: 101,593,860-106,160,500 , GRCh38.p12 chr14: 101,127,523-105,605,042 CDC42BPB, COA8, 133 more genes
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