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Items: 1 to 20 of 166

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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
    nsv7098684copy number variation1nstd102humanPathogenic GRCh38 chr14: 102,573,453-103,575,949 , GRCh37.p13 chr14: 103,039,790-104,042,286 MARK3, GCSHP2, 34 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
    nsv6977472copy number variation1nstd229human GRCh38 chr14: 102,919,601-103,118,100 , GRCh37.p13 chr14: 103,385,938-103,584,437 AMN, CDC42BPB, 3 more genes
    nsv6977149copy number variation1nstd229human GRCh38 chr14: 102,678,201-103,458,700 , GRCh37.p13 chr14: 103,144,538-103,925,037 LBHD2, LOC105370686, 25 more genes
    nsv6976989copy number variation1nstd229human GRCh38 chr14: 102,861,701-102,942,400 , GRCh37.p13 chr14: 103,328,038-103,408,737 RNU6-1316P, CDC42BPB, 2 more genes
    nsv6973824copy number variation1nstd229human GRCh38 chr14: 102,913,149-102,922,366 , GRCh37.p13 chr14: 103,379,486-103,388,703 AMN
    nsv6967743copy number variation1nstd229human GRCh38 chr14: 102,905,880-102,936,668 , GRCh37.p13 chr14: 103,372,217-103,403,005 TRAF3, CDC42BPB, 1 more genes
    nsv6962595copy number variation1nstd229human GRCh38 chr14: 102,918,212-102,920,933 , GRCh37.p13 chr14: 103,384,549-103,387,270 AMN
    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
    nsv6622232copy number variation1nstd224human GRCh37 chr14: 102,881,115-103,396,961 , GRCh38.p12 chr14: 102,414,778-102,930,624 RPL23AP11, LOC105370680, 12 more genes
    nsv6496729copy number variation1nstd223human GRCh38 chr14: 102,822,626-102,957,863 , GRCh37.p13 chr14: 103,288,963-103,424,200 TRAF3, AMN, 2 more genes
    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
    nsv6291566copy number variation1nstd102humannot provided GRCh37 chr14: 102,871,245-103,645,036 , GRCh38.p12 chr14: 102,404,908-103,178,699 RPL21P12, RPL23AP11, 20 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
    nsv6133121copy number variation1nstd213human GRCh37 chr14: 103,220,000-103,460,001 , GRCh38.p12 chr14: 102,753,663-102,993,664 TRAF3, CDC42BPB, 2 more genes
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