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Items: 1 to 20 of 175

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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
    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
    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
    nsv6973992copy number variation1nstd229human GRCh38 chr14: 102,974,701-103,226,700 , GRCh37.p13 chr14: 103,441,038-103,693,037 TNFAIP2, RPL21P12, 9 more genes
    nsv6969606copy number variation1nstd229human GRCh38 chr14: 103,038,255-103,449,234 , GRCh37.p13 chr14: 103,504,592-103,915,571 GCSHP2, LOC105370685, 21 more genes
    nsv6963033copy number variation1nstd229human GRCh38 chr14: 103,114,672-103,119,861 , GRCh37.p13 chr14: 103,581,009-103,586,198 LINC00677, TNFAIP2
    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
    nsv6513714copy number variation1nstd223human GRCh38 chr14: 103,065,408-103,252,792 , GRCh37.p13 chr14: 103,531,745-103,719,129 RPL21P13, EXOC3L4, 8 more genes
    nsv6503574copy number variation1nstd223human GRCh38 chr14: 103,120,812-103,121,138 , GRCh37.p13 chr14: 103,587,149-103,587,475 LINC00677, TNFAIP2
    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
    nsv5498590copy number variation1nstd206human GRCh38 chr14: 80,522,636-106,763,637 , GRCh37.p13 chr14: 80,988,980-106,929,356 , RPS18P2, 713 more genes
    nsv5494004copy number variation1nstd206human GRCh38 chr14: 103,118,975-103,119,524 , GRCh37.p13 chr14: 103,585,312-103,585,861 LINC00677, TNFAIP2
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