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Items: 1 to 20 of 172

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6315273copy number variation1nstd102humanUncertain significance GRCh37 chr16: 30,194,730-30,200,398 , GRCh38.p12 chr16: 30,183,409-30,189,077 CORO1A, CORO1A-AS1
    nsv3905855copy number variation1nstd102humanPathogenic GRCh37 chr16: 21,596,299-30,399,167 , GRCh38.p12 chr16: 21,584,978-30,387,846 CORO1A, LOC107984874, 217 more genes
    nsv3913702copy number variation1nstd102humanPathogenic NCBI36 chr16: 28,311,654-30,239,515 , GRCh37 chr16: 28,404,153-30,332,014 , GRCh38 chr16: 28,392,832-30,320,693 CORO1A, SPN, 94 more genes
    nsv6637500copy number variation1nstd102humanPathogenic GRCh37 chr16: 28,466,731-30,321,320 , GRCh38.p12 chr16: 28,455,410-30,309,999 CORO1A, CA5AP1, 92 more genes
    nsv3915125copy number variation1nstd102humanPathogenic GRCh38 chr16: 28,456,967-30,295,107 , GRCh37 chr16: 28,468,288-30,306,428 , NCBI36 chr16: 28,375,789-30,213,929 CORO1A, SULT1A1, 92 more genes
    nsv3924589copy number variation1nstd102humanPathogenic NCBI36 chr16: 28,310,915-30,104,908 , GRCh37.p13 chr16: 28,403,414-30,197,407 , GRCh38.p12 chr16: 28,392,093-30,186,086 CORO1A, MIR4517, 86 more genes
    nsv3920951copy number variation1nstd102humanPathogenic NCBI36 chr16: 28,311,654-30,104,842 , GRCh37 chr16: 28,404,153-30,197,341 , GRCh38 chr16: 28,392,832-30,186,020 CORO1A, TBX6, 86 more genes
    nsv3898101copy number variation1nstd102humanPathogenic GRCh37 chr16: 28,486,693-30,197,290 , GRCh38.p12 chr16: 28,475,372-30,185,969 CORO1A, TAOK2, 83 more genes
    nsv3915205copy number variation1nstd102humanPathogenic NCBI36 chr16: 28,406,323-30,104,908 , GRCh37.p13 chr16: 28,498,822-30,197,407 , GRCh38.p12 chr16: 28,487,501-30,186,086 CORO1A, TMEM219, 83 more genes
    nsv3923420copy number variation1nstd102humanPathogenic NCBI36 chr16: 28,450,605-30,102,254 , GRCh37 chr16: 28,543,104-30,194,753 , GRCh38 chr16: 28,531,783-30,183,432 CORO1A, KCTD13, 80 more genes
    nsv4349623copy number variation1nstd102humanPathogenic GRCh37 chr16: 29,042,050-30,199,025 , GRCh38.p12 chr16: 29,030,729-30,187,704 CORO1A, LOC606724, 56 more genes
    nsv3911651copy number variation1nstd102humanPathogenic NCBI36 chr16: 29,500,284-30,610,734 , GRCh38 chr16: 29,581,462-30,691,912 , GRCh37 chr16: 29,592,783-30,703,233 CORO1A, PPP4C, 71 more genes
    nsv3894871copy number variation1nstd102humanPathogenic GRCh37 chr16: 29,351,826-30,332,071 , GRCh38.p12 chr16: 29,340,505-30,320,750 CORO1A, PAGR1, 57 more genes
    nsv3892469copy number variation1nstd102humanPathogenic GRCh37 chr16: 29,432,212-30,339,520 , GRCh38.p12 chr16: 29,420,891-30,328,199 CORO1A, BOLA2B, 55 more genes
    nsv6637734copy number variation1nstd102humanPathogenic GRCh37 chr16: 29,432,213-30,240,227 , GRCh38.p12 chr16: 29,420,892-30,228,906 CORO1A, SLX1B, 54 more genes
    nsv3906573copy number variation1nstd102humanPathogenic GRCh37 chr16: 29,412,503-30,215,621 , GRCh38.p12 chr16: 29,401,182-30,204,300 CORO1A, CDIPTOSP, 53 more genes
    nsv3893080copy number variation1nstd102humanPathogenic GRCh37 chr16: 29,567,295-30,344,958 , GRCh38.p12 chr16: 29,555,974-30,333,637 CORO1A, YPEL3-DT, 46 more genes
    nsv5980454copy number variation1nstd102humanPathogenic GRCh37 chr16: 29,545,794-30,307,472 , GRCh38.p12 chr16: 29,534,473-30,296,151 CORO1A, LOC105371167, 46 more genes
    nsv3911982copy number variation1nstd102humanPathogenic GRCh37 chr16: 29,439,269-30,197,341 , NCBI36 chr16: 29,346,770-30,104,842 , GRCh38 chr16: 29,427,948-30,186,020 CORO1A, C16orf54, 47 more genes
    nsv3922171copy number variation1nstd102humanPathogenic NCBI36 chr16: 29,474,796-30,227,808 , GRCh37 chr16: 29,567,295-30,320,307 , GRCh38 chr16: 29,555,974-30,308,986 CORO1A, QPRT, 46 more genes
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