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Items: 1 to 20 of 51

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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 NEIL1, 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 NEIL1, 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 NEIL1, SNX33, 209 more genes
    nsv6637477copy number variation1nstd102humanPathogenic GRCh37 chr15: 74,353,736-77,884,397 , GRCh38.p12 chr15: 74,061,395-77,592,055 NEIL1, PTPN9, 96 more genes
    nsv7137210copy number variation1nstd102humanPathogenic GRCh37 chr15: 72,943,184-76,085,232 , GRCh38.p12 chr15: 72,650,843-75,792,891 NEIL1, LOC105370892, 99 more genes
    nsv3895410copy number variation1nstd102humanPathogenic GRCh37 chr15: 72,943,184-76,072,324 , GRCh38.p12 chr15: 72,650,843-75,779,983 NEIL1, 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 NEIL1, 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 NEIL1, CYP1A1, 88 more genes
    nsv6309590copy number variation1nstd102humanPathogenic GRCh37 chr15: 72,978,569-75,722,716 , GRCh38.p12 chr15: 72,686,228-75,430,375 NEIL1, NPM1P42, 82 more genes
    nsv6315505copy number variation1nstd102humanPathogenic GRCh37 chr15: 74,398,068-76,054,094 , GRCh38.p12 chr15: 74,105,727-75,761,753 NEIL1, RPL36AP45, 62 more genes
    nsv4729106copy number variation1nstd102humanPathogenic GRCh37 chr15: 74,398,162-76,054,094 , GRCh38.p12 chr15: 74,105,821-75,761,753 NEIL1, 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 NEIL1, MIR631, 60 more genes
    nsv3895297copy number variation1nstd102humanPathogenic GRCh37 chr15: 75,078,195-75,862,756 , GRCh38.p12 chr15: 74,785,854-75,570,415 NEIL1, FAM219B, 33 more genes
    nsv5380975copy number variation1nstd102humanPathogenic GRCh37 chr15: 75,596,353-76,103,430 , GRCh38.p12 chr15: 75,304,012-75,811,089 NEIL1, RPL13P4, 20 more genes
    nsv3916409copy number variation1nstd102humanPathogenic NCBI36 chr15: 73,322,401-73,827,604 , GRCh37.p13 chr15: 75,535,348-76,040,549 , GRCh38.p12 chr15: 75,243,007-75,748,208 NEIL1, DNM1P34, 21 more genes
    nsv4349273copy number variation1nstd102humanPathogenic GRCh37 chr15: 75,648,132-76,102,251 , GRCh38.p12 chr15: 75,355,791-75,809,910 NEIL1, SNUPN, 17 more genes
    nsv491514copy number variation1nstd45humanPathogenic GRCh38.p12 chr15: 72,671,374-75,680,568 , GRCh37 chr15: 72,963,715-75,972,909 NEIL1, BBS4, 91 more genes
    nsv3900281copy number variation1nstd102humanPathogenic GRCh37 chr15: 20,016,811-102,493,540 , GRCh38.p12 chr15: 19,811,558-101,953,337 NEIL1, MYZAP, 1750 more genes
    nsv3913581copy number variation1nstd102humanPathogenic NCBI36 chr15: 18,323,354-100,338,915 , GRCh37.p13 chr15: 20,063,340-102,521,392 , GRCh38.p12 chr15: 19,858,087-101,981,189 NEIL1, MIR4513, 1754 more genes
    nsv3904086copy number variation1nstd102humanPathogenic GRCh37 chr15: 20,071,673-102,461,162 , GRCh38.p12 chr15: 19,866,420-101,920,959 NEIL1, TMEM202, 1747 more genes
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