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Items: 1 to 20 of 319

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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
    nsv7145909copy number variation1nstd232human GRCh37.p13 chr14: 103,988,286-103,988,357 , GRCh38.p12 chr14: 103,521,949-103,522,020 CKB
    nsv7141106copy number variation1nstd232human GRCh37.p13 chr14: 103,986,378-103,986,456 , GRCh38.p12 chr14: 103,520,041-103,520,119 CKB
    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
    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
    nsv6975759copy number variation1nstd229human GRCh38 chr14: 103,094,284-103,544,082 , GRCh37.p13 chr14: 103,560,621-104,010,419 LINC00605, EIF5-DT, 21 more genes
    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
    nsv6958191copy number variation1nstd229human GRCh38 chr14: 103,523,301-103,526,000 , GRCh37.p13 chr14: 103,989,638-103,992,337 CKB
    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
    nsv6622435copy number variation1nstd224human GRCh37 chr14: 103,986,500-104,006,693 , GRCh38.p12 chr14: 103,520,163-103,540,356 TRMT61A, CKB
    nsv6622347copy number variation1nstd224human GRCh37 chr14: 103,987,140-104,006,693 , GRCh38.p12 chr14: 103,520,803-103,540,356 CKB, TRMT61A
    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
    nsv5498590copy number variation1nstd206human GRCh38 chr14: 80,522,636-106,763,637 , GRCh37.p13 chr14: 80,988,980-106,929,356 , RPS18P2, 713 more genes
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