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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3911407copy number variation1nstd102humanLikely benign NCBI36 chr15: 72,803,624-72,836,154 , GRCh38 chr15: 74,724,230-74,756,760 , GRCh37 chr15: 75,016,571-75,049,101 CYP1A1, CYP1A2
    nsv3916249copy number variation1nstd102humanPathogenic NCBI36 chr15: 21,173,967-100,338,915 , GRCh37.p13 chr15: 23,622,526-102,521,392 , GRCh38.p12 chr15: 23,377,379-101,981,189 CYP1A1, H3P40, 1616 more genes
    nsv3919468copy number variation1nstd102humanPathogenic NCBI36 chr15: 26,996,912-100,338,915 , GRCh37.p13 chr15: 29,209,620-102,521,392 , GRCh38.p12 chr15: 28,917,417-101,981,189 CYP1A1, RNU6-18P, 1442 more genes
    nsv3913942copy number variation1nstd102humanPathogenic GRCh38 chr15: 70,025,300-78,705,993 , NCBI36 chr15: 68,104,693-76,785,390 , GRCh37 chr15: 70,317,639-78,998,335 CYP1A1, SNX33, 209 more genes
    nsv6637477copy number variation1nstd102humanPathogenic GRCh37 chr15: 74,353,736-77,884,397 , GRCh38.p12 chr15: 74,061,395-77,592,055 CYP1A1, PTPN9, 96 more genes
    nsv7137210copy number variation1nstd102humanPathogenic GRCh37 chr15: 72,943,184-76,085,232 , GRCh38.p12 chr15: 72,650,843-75,792,891 CYP1A1, LOC105370892, 99 more genes
    nsv3895410copy number variation1nstd102humanPathogenic GRCh37 chr15: 72,943,184-76,072,324 , GRCh38.p12 chr15: 72,650,843-75,779,983 CYP1A1, UBL7-DT, 97 more genes
    nsv3920020copy number variation1nstd102humanPathogenic GRCh38 chr15: 72,685,231-75,727,625 , NCBI36 chr15: 70,764,625-73,807,021 , GRCh37 chr15: 72,977,572-76,019,966 CYP1A1, STRA6, 91 more genes
    nsv3914896copy number variation1nstd102humanPathogenic GRCh37 chr15: 72,963,970-75,954,617 , GRCh38 chr15: 72,671,629-75,662,276 , NCBI36 chr15: 70,751,023-73,741,672 CYP1A1, INSYN1-AS1, 88 more genes
    nsv6309590copy number variation1nstd102humanPathogenic GRCh37 chr15: 72,978,569-75,722,716 , GRCh38.p12 chr15: 72,686,228-75,430,375 CYP1A1, NPM1P42, 82 more genes
    nsv3905553copy number variation2nstd102humanPathogenic GRCh37 chr15: 72,943,184-75,567,198 , GRCh38.p12 chr15: 72,650,843-75,274,857 CYP1A1, SEMA7A, 74 more genes
    nsv4455687copy number variation1nstd102humanPathogenic GRCh37 chr15: 72,926,922-75,544,524 , GRCh38.p12 chr15: 72,634,581-75,252,183 CYP1A1, SCAMP2, 74 more genes
    nsv3903760copy number variation1nstd102humanPathogenic GRCh37 chr15: 72,958,539-75,569,605 , GRCh38.p12 chr15: 72,666,198-75,277,264 CYP1A1, LOC105370893, 73 more genes
    nsv3888972copy number variation1nstd102humanPathogenic GRCh37 chr15: 72,958,539-75,569,605 , GRCh38.p12 chr15: 72,666,198-75,277,264 CYP1A1, NEO1, 73 more genes
    nsv4455940copy number variation1nstd102humanPathogenic GRCh37 chr15: 72,943,184-75,544,524 , GRCh38.p12 chr15: 72,650,843-75,252,183 CYP1A1, TBC1D21, 72 more genes
    nsv3914282copy number variation1nstd102humanPathogenic NCBI36 chr15: 70,751,023-73,322,383 , GRCh37 chr15: 72,963,970-75,535,330 , GRCh38 chr15: 72,671,629-75,242,989 CYP1A1, CLK3, 69 more genes
    nsv6315505copy number variation1nstd102humanPathogenic GRCh37 chr15: 74,398,068-76,054,094 , GRCh38.p12 chr15: 74,105,727-75,761,753 CYP1A1, RPL36AP45, 62 more genes
    nsv4729106copy number variation1nstd102humanPathogenic GRCh37 chr15: 74,398,162-76,054,094 , GRCh38.p12 chr15: 74,105,821-75,761,753 CYP1A1, FAM219B, 62 more genes
    nsv3911951copy number variation1nstd102humanPathogenic NCBI36 chr15: 72,186,358-73,827,604 , GRCh37.p13 chr15: 74,399,305-76,040,549 , GRCh38.p12 chr15: 74,106,964-75,748,208 CYP1A1, NEIL1, 60 more genes
    nsv491514copy number variation1nstd45humanPathogenic GRCh38.p12 chr15: 72,671,374-75,680,568 , GRCh37 chr15: 72,963,715-75,972,909 CYP1A1, BBS4, 91 more genes
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