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Items: 1 to 20 of 333

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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
    nsv7147374copy number variation1nstd232human GRCh37.p13 chr14: 105,241,339-105,241,410 , GRCh38.p12 chr14: 104,775,002-104,775,073 AKT1
    nsv7145966copy number variation1nstd232human GRCh37.p13 chr14: 105,239,716-105,239,790 , GRCh38.p12 chr14: 104,773,379-104,773,453 AKT1
    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
    nsv7094484copy number variation1nstd102humanUncertain significance GRCh37 chr14: 105,258,915-105,268,803 , GRCh38.p12 chr14: 104,792,578-104,802,466 AKT1, ZBTB42
    nsv7094483copy number variation1nstd102humanUncertain significance GRCh37 chr14: 105,236,678-105,258,980 , GRCh38.p12 chr14: 104,770,341-104,792,643 LOC102723342, AKT1
    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
    nsv6963343copy number variation1nstd229human GRCh38 chr14: 104,782,003-104,804,453 , GRCh37.p13 chr14: 105,248,340-105,270,790 ZBTB42, AKT1
    nsv6962520copy number variation1nstd229human GRCh38 chr14: 104,790,324-104,800,160 , GRCh37.p13 chr14: 105,256,661-105,266,497 ZBTB42, AKT1
    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
    nsv6508500copy number variation1nstd223human GRCh38 chr14: 104,782,003-104,804,451 , GRCh37.p13 chr14: 105,248,340-105,270,788 ZBTB42, AKT1
    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
    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
    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
    nsv6132861copy number variation1nstd213human GRCh37 chr14: 104,890,000-106,040,001 , GRCh38.p12 chr14: 104,423,663-105,573,664 AKT1, CRIP1, 40 more genes
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