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Items: 7

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    Number of Variants: 7

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv889261copy number variation57nstd71human NCBI36 chr7: 141,410,335-141,439,888 , GRCh37.p13 chr7|NW_003571040.1: 206,017-235,570 , GRCh37.p13 chr7: 141,763,866-141,793,419 , GRCh38.p12 chr7|NT_187562.1: 25,946-55,499 , GRCh38.p12 chr7: 142,064,066-142,093,619 MGAM
    nsv879279copy number variation1nstd71human NCBI36 chr4: 69,064,675-69,127,630 , GRCh37.p13 chr4: 69,382,080-69,445,035 , GRCh38.p12 chr4: 68,516,362-68,579,317 UGT2B17, UGT2B29P
    nsv871196copy number variation88nstd71human NCBI36 chr1: 12,777,429-12,810,136 , GRCh37.p13 chr1: 12,854,842-12,887,549 , GRCh38.p12 chr1: 12,794,693-12,827,690 PRAMEF11, PRAMEF1, 1 more genes
    nsv883875copy number variation28nstd71human NCBI36 chr6: 29,982,594-30,003,090 , GRCh37.p13 chr6|NT_167246.1: 1,168,792-1,189,318 , GRCh37.p13 chr6: 29,874,615-29,895,111 , GRCh38.p12 chr6: 29,906,838-29,927,334 , GRCh38.p12 chr6|NT_167246.2: 1,163,172-1,183,698 MCCD1P1, LOC353008, 4 more genes
    nsv887509copy number variation176nstd71human NCBI36 chr7: 8,791,785-8,833,529 , GRCh37.p13 chr7: 8,825,260-8,867,004 , GRCh38.p12 chr7: 8,785,630-8,827,374 0
    nsv886198copy number variation304nstd71human NCBI36 chr6: 77,073,066-77,088,077 , GRCh37.p13 chr6: 77,016,346-77,031,357 , GRCh38.p12 chr6: 76,306,629-76,321,640 0
    nsv901399copy number variation3nstd71human NCBI36 chr14: 19,335,041-19,494,891 , GRCh37.p13 chr14: 20,265,201-20,425,051 , GRCh38.p12 chr14: 19,797,042-19,956,892 OR4K1, OR4K4P, 8 more genes
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