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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098902copy number variation1nstd102humanPathogenic GRCh37 chr16: 86,544,176-88,110,267 , GRCh38.p12 chr16: 86,510,570-88,076,661 LOC107984816, BANP, 33 more genes
    nsv7094605copy number variation1nstd102humanUncertain significance GRCh37 chr16: 85,936,622-86,602,447 , GRCh38.p12 chr16: 85,903,016-86,568,841 LINC00917, RPL7AP63, 16 more genes
    nsv6997821copy number variation1nstd229human GRCh38 chr16: 86,536,050-86,538,911 , GRCh37.p13 chr16: 86,569,656-86,572,517 MTHFSD
    nsv6996222copy number variation1nstd229human GRCh38 chr16: 86,324,301-86,588,300 , GRCh37.p13 chr16: 86,357,907-86,621,906 FOXF1, FENDRR, 8 more genes
    nsv6986438copy number variation1nstd229human GRCh38 chr16: 86,527,055-86,529,124 , GRCh37.p13 chr16: 86,560,661-86,562,730 MTHFSD
    nsv6985793copy number variation1nstd229human GRCh38 chr16: 86,497,601-86,603,500 , GRCh37.p13 chr16: 86,531,207-86,637,106 FOXL1, MTHFSD, 6 more genes
    nsv6984082copy number variation1nstd229human GRCh38 chr16: 86,545,375-86,551,099 , GRCh37.p13 chr16: 86,578,981-86,584,705 MTHFSD
    nsv6982860copy number variation1nstd229human GRCh38 chr16: 86,526,128-86,528,890 , GRCh37.p13 chr16: 86,559,734-86,562,496 RPL7AP63, MTHFSD
    nsv6981623copy number variation1nstd229human GRCh38 chr16: 86,533,311-86,542,631 , GRCh37.p13 chr16: 86,566,917-86,576,237 MTHFSD
    nsv6980449copy number variation1nstd229human GRCh38 chr16: 86,553,701-86,560,600 , GRCh37.p13 chr16: 86,587,307-86,594,206 MTHFSD, FLJ30679
    nsv6980129copy number variation1nstd229human GRCh38 chr16: 86,464,201-86,591,400 , GRCh37.p13 chr16: 86,497,807-86,625,006 RPL7AP63, MTHFSD, 6 more genes
    nsv6978518copy number variation1nstd229human GRCh38 chr16: 86,555,601-86,559,200 , GRCh37.p13 chr16: 86,589,207-86,592,806 FLJ30679, MTHFSD
    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
    nsv6623942copy number variation1nstd224human GRCh37 chr16: 86,290,512-86,710,660 , GRCh38.p12 chr16: 86,256,906-86,677,054 LINC02135, FENDRR, 10 more genes
    nsv6623790copy number variation1nstd224human GRCh37 chr16: 86,189,977-87,237,863 , GRCh38.p12 chr16: 86,156,371-87,204,257 FOXC2, FENDRR, 17 more genes
    nsv6514460copy number variation1nstd223human GRCh38 chr16: 86,533,712-86,534,897 , GRCh37.p13 chr16: 86,567,318-86,568,503 MTHFSD
    nsv6510920copy number variation1nstd223human GRCh38 chr16: 86,529,384-86,529,677 , GRCh37.p13 chr16: 86,562,990-86,563,283 MTHFSD
    nsv6505910copy number variation1nstd223human GRCh38 chr16: 86,526,128-86,528,885 , GRCh37.p13 chr16: 86,559,734-86,562,491 MTHFSD, RPL7AP63
    nsv6505596copy number variation1nstd223human GRCh38 chr16: 86,548,608-86,549,224 , GRCh37.p13 chr16: 86,582,214-86,582,830 MTHFSD
    nsv6502382copy number variation1nstd223human GRCh38 chr16: 86,551,098-86,551,529 , GRCh37.p13 chr16: 86,584,704-86,585,135 MTHFSD
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