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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7141559copy number variation1nstd232human GRCh37.p13 chr16: 80,604,439-80,604,573 , GRCh38.p12 chr16: 80,570,542-80,570,676 LINC01227
    nsv7072039inversion1nstd229human GRCh38 chr16: 79,903,600-82,537,648 , GRCh37.p13 chr16: 79,937,497-82,571,253 RN7SKP176, LOC105371357, 34 more genes
    nsv7070808inversion1nstd229human GRCh38 chr16: 79,903,594-82,532,651 , GRCh37.p13 chr16: 79,937,491-82,566,256 DYNLRB2, RNU6-1191P, 34 more genes
    nsv7069467inversion1nstd229human GRCh38 chr16: 77,603,047-81,438,175 , GRCh37.p13 chr16: 77,636,944-81,471,780 ATMIN, WWOX, 39 more genes
    nsv6995966copy number variation1nstd229human GRCh38 chr16: 80,497,813-80,587,021 , GRCh37.p13 chr16: 80,531,710-80,620,918 DYNLRB2, LINC01227, 1 more genes
    nsv6994608copy number variation1nstd229human GRCh38 chr16: 76,392,054-84,158,971 , GRCh37.p13 chr16: 76,425,951-84,192,576 , MAFTRR, 87 more genes
    nsv6993656copy number variation1nstd229human GRCh38 chr16: 80,348,419-81,288,034 , GRCh37.p13 chr16: 80,382,316-81,321,639 BCO1, RNU6-1191P, 13 more genes
    nsv6992339copy number variation1nstd229human GRCh38 chr16: 80,568,285-80,598,708 , GRCh37.p13 chr16: 80,602,182-80,632,605 CDYL2, LINC01227
    nsv6983964copy number variation1nstd229human GRCh38 chr16: 80,542,988-80,577,040 , GRCh37.p13 chr16: 80,576,885-80,610,937 DYNLRB2-AS1, LINC01227, 1 more genes
    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
    nsv6515234copy number variation1nstd223human GRCh38 chr16: 80,566,499-80,567,501 , GRCh37.p13 chr16: 80,600,396-80,601,398 LINC01227
    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
    nsv6314107copy number variation1nstd102humanUncertain significance GRCh37 chr16: 77,960,664-81,429,258 , GRCh38.p12 chr16: 77,926,767-81,395,653 ARLNC1, MAF, 36 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
    nsv6273881copy number variation1nstd214human GRCh38 chr16: 80,568,371-80,568,438 , GRCh37.p13 chr16: 80,602,268-80,602,335 LINC01227
    nsv6203627copy number variation1nstd214human GRCh38 chr16: 80,570,542-80,570,676 , GRCh37.p13 chr16: 80,604,439-80,604,573 LINC01227
    nsv6195745copy number variation1nstd214human GRCh38 chr16: 80,568,297-80,568,398 , GRCh37.p13 chr16: 80,602,194-80,602,295 LINC01227
    nsv6188938copy number variation1nstd214human GRCh38 chr16: 80,570,552-80,570,686 , GRCh37.p13 chr16: 80,604,449-80,604,583 LINC01227
    nsv6133211copy number variation1nstd213human GRCh37 chr16: 79,110,000-80,850,001 , GRCh38.p12 chr16: 79,076,103-80,816,104 MAF, WWOX, 12 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
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