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Items: 1 to 20 of 154

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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
    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
    nsv6970176copy number variation1nstd229human GRCh38 chr14: 102,316,874-102,383,598 , GRCh37.p13 chr14: 102,783,211-102,849,935 TRI-AAT5-4, TECPR2, 2 more genes
    nsv6963986copy number variation1nstd229human GRCh38 chr14: 102,304,701-102,348,800 , GRCh37.p13 chr14: 102,771,038-102,815,137 TRI-AAT5-4, CINP, 2 more genes
    nsv6962550copy number variation1nstd229human GRCh38 chr14: 102,336,413-102,351,250 , GRCh37.p13 chr14: 102,802,750-102,817,587 CINP, ZNF839
    nsv6960497copy number variation1nstd229human GRCh38 chr14: 102,155,025-102,356,399 , GRCh37.p13 chr14: 102,621,362-102,822,736 WDR20, ZNF839, 4 more genes
    nsv6959347copy number variation1nstd229human GRCh38 chr14: 102,147,957-102,398,368 , GRCh37.p13 chr14: 102,614,294-102,864,705 TRI-AAT5-4, LOC105370677, 5 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
    nsv6584504inversion1nstd223human GRCh38 chr14: 102,345,858-102,346,833 , GRCh37.p13 chr14: 102,812,195-102,813,170 CINP
    nsv6578705inversion1nstd223human GRCh38 chr14: 102,345,959-102,346,481 , GRCh37.p13 chr14: 102,812,296-102,812,818 CINP
    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
    nsv6314834copy number variation1nstd102humanUncertain significance GRCh37 chr14: 102,829,248-102,968,819 , GRCh38.p12 chr14: 102,362,911-102,502,482 ANKRD9, CINP, 2 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
    nsv5502379copy number variation1nstd206human GRCh38 chr14: 102,354,681-102,355,014 , GRCh37.p13 chr14: 102,821,018-102,821,351 CINP
    nsv5498590copy number variation1nstd206human GRCh38 chr14: 80,522,636-106,763,637 , GRCh37.p13 chr14: 80,988,980-106,929,356 , RPS18P2, 713 more genes
    nsv5005015copy number variation1nstd200human GRCh38 chr14: 102,348,044-102,350,699 , GRCh37.p13 chr14: 102,814,381-102,817,036 CINP
    nsv5005014copy number variation1nstd200human GRCh38 chr14: 102,297,519-102,369,284 , GRCh37.p13 chr14: 102,763,856-102,835,621 TRI-AAT5-4, CINP, 3 more genes
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