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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6635853copy number variation8nstd227human GRCh37 chr16: 32,165,782-33,795,687 , GRCh38.p12 chr16: 32,154,461-33,993,220 TP53TG3, ABCD1P3, 56 more genes
    nsv6635187copy number variation2nstd227human GRCh37 chr16: 32,165,782-34,194,635 , GRCh38.p12 chr16: 32,154,461-34,960,264 TP53TG3, ABCD1P3, 70 more genes
    nsv6623601copy number variation1nstd224human GRCh37 chr16: 32,096,969-32,650,542 , GRCh38.p12 chr16: 32,085,648-32,639,221 ACTR3BP3, ABCD1P3, 12 more genes
    nsv6588482inversion1nstd223human GRCh38 chr16: 32,115,700-32,812,110 , GRCh37.p13 chr16: 32,127,021-32,823,431 HERC2P5, ABHD17AP7, 18 more genes
    nsv6306935copy number variation1nstd186human GRCh37 chr16: 32,161,807-32,362,521 , GRCh38.p12 chr16: 32,150,486-32,351,200 LOC390705, ABHD17AP8, 5 more genes
    nsv6145332copy number variation1nstd206human GRCh38 chr16: 32,067,486-33,310,450 , GRCh37.p13 chr16: 32,078,807-33,225,916 LOC112268180, HERC2P5, 33 more genes
    nsv6145080copy number variation1nstd206human GRCh38 chr16: 32,150,486-32,351,200 , GRCh37.p13 chr16: 32,161,807-32,362,521 LOC390705, ABHD17AP8, 5 more genes
    nsv5588888copy number variation1nstd207human GRCh38 chr16: 32,168,259-32,170,062 , GRCh37.p13 chr16: 32,179,580-32,181,383 HERC2P4
    nsv5301051copy number variation1nstd204human GRCh38.p13 chr16: 31,854,272-34,660,717 , GRCh37.p13 chr16: 31,865,593-34,023,151 , BCAP31P2, 80 more genes
    nsv5279763copy number variation1nstd204human GRCh38.p13 chr16: 32,160,101-32,190,400 , GRCh37.p13 chr16: 32,171,422-32,201,721 HERC2P4
    nsv5277849copy number variation1nstd204human GRCh38.p13 chr16: 32,173,001-32,201,700 , GRCh37.p13 chr16: 32,184,322-32,213,021 HERC2P4, ABHD17AP8
    nsv5271608copy number variation1nstd204human GRCh38.p13 chr16: 32,145,301-32,201,100 , GRCh37.p13 chr16: 32,156,622-32,212,421 HERC2P4, ABHD17AP8
    nsv5268784copy number variation1nstd204human GRCh38.p13 chr16: 32,159,601-32,215,000 , GRCh37.p13 chr16: 32,170,922-32,226,321 HERC2P4, ABHD17AP8
    nsv5266144copy number variation1nstd204human GRCh38.p13 chr16: 32,141,401-32,222,300 , GRCh37.p13 chr16: 32,152,722-32,233,621 HERC2P4, ABHD17AP8
    nsv5260716copy number variation1nstd204human GRCh38.p13 chr16: 32,178,201-32,181,600 , GRCh37.p13 chr16: 32,189,522-32,192,921 HERC2P4
    nsv4994635copy number variation1nstd200human GRCh38 chr16: 32,085,579-33,029,092 , GRCh37.p13 chr16: 32,096,900-33,040,413 IGHV2OR16-5, ABHD17AP7, 27 more genes
    nsv4749427copy number variation1nstd199human GRCh37 chr16: 29,238,132-88,226,311 , GRCh38.p12 chr16: 29,226,811-88,192,705 , ITGAM, 1076 more genes
    nsv4708826copy number variation1nstd195human GRCh37 chr16: 32,178,051-32,183,151 , GRCh38.p12 chr16: 32,166,730-32,171,830 HERC2P4
    nsv4708314copy number variation1nstd195human GRCh37 chr16: 32,179,201-32,183,151 , GRCh38.p12 chr16: 32,167,880-32,171,830 HERC2P4
    nsv4702567copy number variation1nstd195human GRCh37 chr16: 32,179,501-32,183,151 , GRCh38.p12 chr16: 32,168,180-32,171,830 HERC2P4
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