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Items: 1 to 20 of 94

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv4864104copy number variation1nstd200human GRCh37 chr16: 31,476,589-31,489,409 , GRCh38.p12 chr16: 31,465,268-31,478,088 ARMC5, TGFB1I1
    nsv4749427copy number variation1nstd199human GRCh37 chr16: 29,238,132-88,226,311 , GRCh38.p12 chr16: 29,226,811-88,192,705 , ITGAM, 1076 more genes
    nsv4729988copy number variation1nstd102humanUncertain significance GRCh37 chr16: 30,350,747-31,905,898 , GRCh38.p12 chr16: 30,339,426-31,894,577 VN1R3, HSD3B7, 89 more genes
    nsv4685985copy number variation1nstd102humanPathogenic GRCh37 chr16: 5,805,001-34,230,001 , GRCh38.p12 chr16: 5,755,000-34,995,630 LOC105371069, PKD1P6-NPIPP1, 654 more genes
    nsv4436312complex substitution1nstd102humanPathogenic GRCh38.p12 chr16: 1,230,041-33,908,091 , GRCh37 chr16: 1,280,042-33,710,558 ABAT, ABCA3, 876 more genes
    nsv4322553inversion1nstd166human GRCh37.p13 chr16: 16,634,964-31,736,102 , GRCh38.p12 chr16: 16,541,107-31,724,781 , ALDOA, 403 more genes
    nsv4240965copy number variation1nstd166human GRCh37.p13 chr16: 31,476,589-31,489,409 , GRCh38.p12 chr16: 31,465,268-31,478,088 TGFB1I1, ARMC5
    nsv3918492copy number variation1nstd102humanPathogenic GRCh37 chr16: 30,703,233-35,147,508 , NCBI36 chr16: 30,610,734-35,005,009 , GRCh38 chr16: 30,691,912-36,160,463 KRBOX5P1, LOC110262331, 213 more genes
    nsv3914248copy number variation1nstd102humanPathogenic GRCh37 chr16: 23,763,368-31,955,076 , GRCh38 chr16: 23,752,047-31,943,755 , NCBI36 chr16: 23,670,869-31,862,577 ZG16, TPRKBP2, 250 more genes
    nsv3913895copy number variation1nstd102humanPathogenic NCBI36 chr16: 24,289,454-33,830,560 , GRCh37.p13 chr16: 24,381,953-33,923,059 , GRCh38.p12 chr16: 24,370,632-34,120,592 ITGAL, CORO1A, 310 more genes
    nsv3909417copy number variation1nstd102humanPathogenic GRCh37 chr16: 88,165-90,163,275 , GRCh38.p12 chr16: 38,165-90,096,867 PRSS53, LINC02134, 1868 more genes
    nsv3906108copy number variation1nstd102humanPathogenic GRCh37 chr16: 61,451-90,294,632 , GRCh38.p12 chr16: 11,451-90,228,224 CKLF, NPIPP1, 1882 more genes
    nsv3905126copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 28,826,162-34,375,007 , GRCh38.p12 chr16: 28,814,841-35,140,636 ALDOA, ATP2A1, 255 more genes
    nsv3904593copy number variation1nstd102humanPathogenic GRCh37 chr16: 69,193-90,274,381 , GRCh38.p12 chr16: 19,193-90,207,973 LOC100128079, LOC105379474, 1879 more genes
    nsv3901410copy number variation1nstd102humanPathogenic GRCh37 chr16: 88,165-90,274,695 , GRCh38.p12 chr16: 38,165-90,208,287 LINC02175, FCSK, 1877 more genes
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