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Items: 1 to 20 of 109

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7068091inversion1nstd229human GRCh38 chr16: 29,736,414-31,610,190 , GRCh37.p13 chr16: 29,747,735-31,621,511 C16orf92, TMEM219, 118 more genes
    nsv6997031copy number variation1nstd229human GRCh38 chr16: 31,465,268-31,478,088 , GRCh37.p13 chr16: 31,476,589-31,489,409 ARMC5, TGFB1I1
    nsv6991978copy number variation1nstd229human GRCh38 chr16: 31,477,016-31,477,382 , GRCh37.p13 chr16: 31,488,337-31,488,703 TGFB1I1
    nsv6991338copy number variation1nstd229human GRCh38 chr16: 31,324,840-31,575,158 , GRCh37.p13 chr16: 31,336,161-31,586,479 YBX3P1, COX6A2, 14 more genes
    nsv6986779copy number variation1nstd229human GRCh38 chr16: 31,466,801-31,475,900 , GRCh37.p13 chr16: 31,478,122-31,487,221 TGFB1I1, ARMC5
    nsv6986477copy number variation1nstd229human GRCh38 chr16: 31,462,493-31,473,165 , GRCh37.p13 chr16: 31,473,814-31,484,486 ARMC5, TGFB1I1
    nsv6983834copy number variation1nstd229human GRCh38 chr16: 31,474,101-31,477,900 , GRCh37.p13 chr16: 31,485,422-31,489,221 TGFB1I1
    nsv6980127copy number variation1nstd229human GRCh38 chr16: 31,261,410-31,863,261 , GRCh37.p13 chr16: 31,272,731-31,874,582 ITGAM, FRG2KP, 24 more genes
    nsv6590041inversion1nstd223human GRCh38 chr16: 29,736,419-31,610,189 , GRCh37.p13 chr16: 29,747,740-31,621,510 MIR762HG, FBXL19, 118 more genes
    nsv6515405copy number variation1nstd223human GRCh38 chr16: 31,471,084-31,594,845 , GRCh37.p13 chr16: 31,482,405-31,606,166 SLC5A2, RUSF1, 7 more genes
    nsv6515348copy number variation1nstd223human GRCh38 chr16: 31,465,268-31,478,088 , GRCh37.p13 chr16: 31,476,589-31,489,409 ARMC5, TGFB1I1
    nsv6500288copy number variation1nstd223human GRCh38 chr16: 31,468,921-31,470,179 , GRCh37.p13 chr16: 31,480,242-31,481,500 TGFB1I1
    nsv6133268copy number variation1nstd213human GRCh37 chr16: 22,710,000-32,010,001 , GRCh38.p12 chr16: 22,698,679-31,998,680 ALDOA, AQP8, 269 more genes
    nsv6133022copy number variation1nstd213human GRCh37 chr16: 30,300,000-32,030,001 , GRCh38.p12 chr16: 30,288,679-32,018,680 COX6A2, CTF1, 91 more genes
    nsv6132984copy number variation1nstd213human GRCh37 chr16: 31,340,000-32,080,001 , GRCh38.p12 chr16: 31,328,679-32,068,680 COX6A2, ITGAD, 31 more genes
    nsv5380192translocation1nstd200human GRCh38 chr16: 31,465,268-31,465,268 , GRCh38 chr16: 31,478,088-31,478,088 , GRCh37.p13 chr16: 31,489,409-31,489,409 , GRCh37.p13 chr16: 31,476,589-31,476,589 ARMC5, TGFB1I1
    nsv5309994copy number variation1nstd204human GRCh38.p13 chr16: 31,465,258-31,478,097 , GRCh37.p13 chr16: 31,476,579-31,489,418 ARMC5, TGFB1I1
    nsv5277124copy number variation1nstd204human GRCh38.p13 chr16: 31,465,118-31,476,468 , GRCh37.p13 chr16: 31,476,439-31,487,789 ARMC5, TGFB1I1
    nsv5040420inversion1nstd200human GRCh38 chr16: 29,736,418-31,610,189 , GRCh37.p13 chr16: 29,747,739-31,621,510 , ZNF668, 119 more genes
    nsv4879933inversion1nstd200human GRCh37 chr16: 29,747,739-31,621,510 , GRCh38.p12 chr16: 29,736,418-31,610,189 , LOC613038, 119 more genes
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