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Items: 1 to 20 of 421

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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
    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
    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
    nsv7062190inversion1nstd229human GRCh38 chr14: 103,555,287-104,539,425 , GRCh37.p13 chr14: 104,021,624-104,966,919 RNU4-68P, MIR203B, 21 more genes
    nsv6975656copy number variation1nstd229human GRCh38 chr14: 104,181,224-104,186,797 , GRCh37.p13 chr14: 104,647,561-104,653,134 KIF26A
    nsv6973256copy number variation1nstd229human GRCh38 chr14: 104,165,051-104,165,713 , GRCh37.p13 chr14: 104,631,388-104,632,050 KIF26A
    nsv6972973copy number variation1nstd229human GRCh38 chr14: 104,164,389-104,168,829 , GRCh37.p13 chr14: 104,630,726-104,635,166 KIF26A
    nsv6969688copy number variation1nstd229human GRCh38 chr14: 104,057,242-104,269,659 , GRCh37.p13 chr14: 104,523,579-104,735,996 ASPG, MIR203A, 4 more genes
    nsv6969344copy number variation1nstd229human GRCh38 chr14: 104,137,894-104,137,933 , GRCh37.p13 chr14: 104,604,231-104,604,270 KIF26A-DT, KIF26A
    nsv6967906copy number variation1nstd229human GRCh38 chr14: 104,058,547-104,336,906 , GRCh37.p13 chr14: 104,524,884-104,803,243 KIF26A-DT, MIR203B, 4 more genes
    nsv6967560copy number variation1nstd229human GRCh38 chr14: 104,129,139-104,172,884 , GRCh37.p13 chr14: 104,595,476-104,639,221 KIF26A, KIF26A-DT
    nsv6964192copy number variation1nstd229human GRCh38 chr14: 104,113,301-104,177,900 , GRCh37.p13 chr14: 104,579,638-104,644,237 KIF26A-DT, KIF26A, 3 more genes
    nsv6963871copy number variation1nstd229human GRCh38 chr14: 104,135,201-104,139,600 , GRCh37.p13 chr14: 104,601,538-104,605,937 KIF26A-DT, KIF26A
    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
    nsv6622436copy number variation1nstd224human GRCh37 chr14: 104,573,577-104,639,499 , GRCh38.p12 chr14: 104,107,240-104,173,162 KIF26A-DT, KIF26A, 3 more genes
    nsv6507831copy number variation1nstd223human GRCh38 chr14: 104,165,559-104,165,663 , GRCh37.p13 chr14: 104,631,896-104,632,000 KIF26A
    nsv6505785copy number variation1nstd223human GRCh38 chr14: 104,058,547-104,336,901 , GRCh37.p13 chr14: 104,524,884-104,803,238 ASPG, MIR203B, 4 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
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