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Items: 1 to 20 of 136

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094683copy number variation1nstd102humanUncertain significance GRCh37 chr16: 65,821,800-72,146,396 , GRCh38.p12 chr16: 65,787,897-72,112,497 TRG-GCC5-1, RNU6-359P, 205 more genes
    nsv7075084inversion1nstd229human GRCh38 chr16: 67,127,296-73,957,488 , GRCh37.p13 chr16: 67,161,199-73,991,387 MIR1538, LINC02136, 187 more genes
    nsv7064268inversion1nstd229human GRCh38 chr16: 69,686,669-74,423,188 , GRCh37.p13 chr16: 69,720,572-74,457,086 LOC102723786, RNU7-90P, 99 more genes
    nsv7059282inversion1nstd229human GRCh38 chr16: 69,511,560-71,175,016 , GRCh37.p13 chr16: 69,545,463-71,208,919 COG4, DDX19B, 42 more genes
    nsv7058675inversion1nstd229human GRCh38 chr16: 67,667,666-75,720,241 , GRCh37.p13 chr16: 67,701,569-75,754,139 RNU6-898P, DPEP2, 199 more genes
    nsv6985777copy number variation1nstd229human GRCh38 chr16: 69,754,866-69,754,903 , GRCh37.p13 chr16: 69,788,769-69,788,806 NOB1, NONOP1
    nsv6980681copy number variation1nstd229human GRCh38 chr16: 69,677,027-69,924,914 , GRCh37.p13 chr16: 69,710,930-69,958,817 NONOP1, SNORD13H, 4 more genes
    nsv6978831copy number variation1nstd229human GRCh38 chr16: 69,483,001-69,919,500 , GRCh37.p13 chr16: 69,516,904-69,953,403 NONOP1, SNORD13H, 6 more genes
    nsv6623740copy number variation1nstd224human GRCh37 chr16: 69,724,465-69,951,291 , GRCh38.p12 chr16: 69,690,562-69,917,388 NQO1, NFAT5, 4 more genes
    nsv6514699copy number variation1nstd223human GRCh38 chr16: 69,738,931-69,786,647 , GRCh37.p13 chr16: 69,772,834-69,820,550 NONOP1, NOB1, 1 more genes
    nsv6315469copy number variation1nstd102humanPathogenic GRCh37 chr16: 68,971,067-74,823,560 , GRCh38.p12 chr16: 68,937,164-74,789,662 ZNF19, RNU7-71P, 128 more genes
    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
    nsv6309922copy number variation1nstd102humanUncertain significance GRCh37 chr16: 69,680,960-72,146,396 , GRCh38.p12 chr16: 69,647,057-72,112,497 CHST4, TAT, 74 more genes
    nsv6133279copy number variation1nstd213human GRCh37 chr16: 69,690,000-69,800,001 , GRCh38.p12 chr16: 69,656,097-69,766,098 NQO1, NFAT5, 4 more genes
    nsv6133200copy number variation1nstd213human GRCh37 chr16: 46,460,000-84,740,001 , GRCh38.p12 chr16: 46,426,088-84,706,395 , AARS1, 674 more genes
    nsv6132998copy number variation1nstd213human GRCh37 chr16: 69,670,000-70,150,001 , GRCh38.p12 chr16: 69,636,097-70,116,098 NQO1, NFAT5, 12 more genes
    nsv5532278copy number variation1nstd206human GRCh38 chr16: 69,677,060-69,924,863 , GRCh37.p13 chr16: 69,710,963-69,958,766 NQO1, NFAT5, 4 more genes
    nsv5263716copy number variation1nstd204human GRCh37.p13 chr16: 69,700,104-69,946,603 , GRCh38.p13 chr16: 69,666,201-69,912,700 NQO1, NFAT5, 4 more genes
    nsv5149624mobile element insertion1nstd203human GRCh38 chr16: 69,753,524-69,753,540 , GRCh37.p13 chr16: 69,787,427-69,787,443 NOB1, NONOP1
    nsv5034683inversion1nstd200human GRCh38 chr16: 60,098,351-77,500,042 , GRCh37.p13 chr16: 60,132,255-77,533,939 , TRG-GCC2-5, 313 more genes
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