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Items: 1 to 20 of 182

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6995898copy number variation1nstd229human GRCh38 chr16: 85,728,662-85,740,739 , GRCh37.p13 chr16: 85,762,268-85,774,345 MIR1910, C16orf74
    nsv6993503copy number variation1nstd229human GRCh38 chr16: 85,728,046-85,756,905 , GRCh37.p13 chr16: 85,761,652-85,790,511 MIR1910, C16orf74
    nsv6985396copy number variation1nstd229human GRCh38 chr16: 85,733,609-85,745,861 , GRCh37.p13 chr16: 85,767,215-85,779,467 MIR1910, C16orf74
    nsv6634465copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 71,610,276-90,354,753 , GRCh38.p12 chr16: 71,576,373-90,228,345 AP1G1, AFG3L1P, 349 more genes
    nsv6590742inversion1nstd223human GRCh38 chr16: 83,952,013-85,834,110 , GRCh37.p13 chr16: 83,985,618-85,867,716 LOC101928502, LOC105371382, 47 more genes
    nsv6515577copy number variation1nstd223human GRCh38 chr16: 85,740,132-85,745,017 , GRCh37.p13 chr16: 85,773,738-85,778,623 C16orf74, MIR1910
    nsv6510334copy number variation1nstd223human GRCh38 chr16: 85,737,639-85,740,424 , GRCh37.p13 chr16: 85,771,245-85,774,030 MIR1910, C16orf74
    nsv6508841copy number variation1nstd223human GRCh38 chr16: 85,732,801-85,758,500 , GRCh37.p13 chr16: 85,766,407-85,792,106 C16orf74, MIR1910
    nsv6500282copy number variation1nstd223human GRCh38 chr16: 85,702,641-85,769,286 , GRCh37.p13 chr16: 85,736,247-85,802,892 MIR1910, C16orf74
    nsv6500212copy number variation1nstd223human GRCh38 chr16: 85,736,894-85,746,143 , GRCh37.p13 chr16: 85,770,500-85,779,749 C16orf74, MIR1910
    nsv6314755copy number variation1nstd102humanPathogenic GRCh37 chr16: 46,503,968-90,155,062 , GRCh38.p12 chr16: 46,470,056-90,088,654 ATMIN, ATP6V0D1, 826 more genes
    nsv6290331copy number variation1nstd102humanPathogenic GRCh37 chr16: 80,386,595-90,163,348 , GRCh38.p12 chr16: 80,352,698-90,096,940 GINS2, TCF25, 220 more genes
    nsv6133286copy number variation1nstd213human GRCh37 chr16: 85,640,000-86,830,001 , GRCh38.p12 chr16: 85,606,394-86,796,395 COX4I1, FOXF1, 32 more genes
    nsv6133284copy number variation1nstd213human GRCh37 chr16: 84,740,000-85,940,001 , GRCh38.p12 chr16: 84,706,394-85,906,395 COX4I1, IRF8, 28 more genes
    nsv6133214copy number variation1nstd213human GRCh37 chr16: 85,100,000-90,290,001 , GRCh38.p12 chr16: 85,066,394-90,223,593 AFG3L1P, APRT, 156 more genes
    nsv6133210copy number variation1nstd213human GRCh37 chr16: 78,970,000-88,180,001 , GRCh38.p12 chr16: 78,936,103-88,146,395 , CA5A, 152 more genes
    nsv5884300copy number variation1nstd209human GRCh38 chr16: 85,738,362-85,740,611 , GRCh37.p13 chr16: 85,771,968-85,774,217 C16orf74, MIR1910
    nsv5530601copy number variation1nstd206human GRCh38 chr16: 85,732,492-85,758,503 , GRCh37.p13 chr16: 85,766,098-85,792,109 MIR1910, C16orf74
    nsv5523948copy number variation1nstd206human GRCh38 chr16: 85,740,055-85,740,547 , GRCh37.p13 chr16: 85,773,661-85,774,153 MIR1910, C16orf74
    nsv5292274copy number variation1nstd204human GRCh38.p13 chr16: 85,732,401-85,748,600 , GRCh37.p13 chr16: 85,766,007-85,782,206 MIR1910, C16orf74
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