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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098897copy number variation1nstd102humanPathogenic GRCh37 chr15: 67,358,491-91,644,328 , GRCh38.p12 chr15: 67,066,153-91,101,098 LINC00933, DNM1P9, 540 more genes
    nsv7069747inversion1nstd229human GRCh38 chr15: 65,994,863-75,247,978 , GRCh37.p13 chr15: 66,287,201-75,540,319 REC114, PARP6, 199 more genes
    nsv7059031inversion1nstd229human GRCh38 chr15: 70,160,153-73,809,878 , GRCh37.p13 chr15: 70,452,492-74,102,219 CD276, LOC107984716, 71 more genes
    nsv6132964copy number variation1nstd213human GRCh37 chr15: 70,890,000-71,180,001 , GRCh38.p12 chr15: 70,597,661-70,887,662 LRRC49, UACA, 7 more genes
    nsv6132961copy number variation1nstd213human GRCh37 chr15: 69,080,000-73,430,001 , GRCh38.p12 chr15: 68,787,661-73,137,660 BBS4, MYO9A, 84 more genes
    nsv5380758copy number variation2nstd102humanUncertain significance GRCh37 chr15: 32,964,879-91,358,519 , GRCh38.p12 chr15: 32,672,678-90,815,289 LOC105370794, HNRNPA1P45, 1173 more genes
    nsv4728893copy number variation1nstd102humanLikely pathogenic GRCh37 chr15: 70,268,937-74,098,081 , GRCh38.p12 chr15: 69,976,598-73,805,740 BBS4, FKBP1AP2, 75 more genes
    nsv4709927copy number variation1nstd195human GRCh38.p12 chr15: 70,735,012-70,984,712 , GRCh37 chr15: 71,027,351-71,277,051 LRRC49, UACA, 4 more genes
    nsv4678891copy number variation1nstd189human GRCh37.p13 chr15: 70,843,178-71,191,788 , GRCh38.p12 chr15: 70,550,839-70,899,449 LRRC49, UACA, 9 more genes
    nsv4338323sequence alteration1nstd166human GRCh37.p13 chr15: 69,446,476-72,211,091 , GRCh38.p12 chr15: 69,154,137-71,918,750 , MYO9A, 45 more genes
    nsv3922157copy number variation1nstd102humanUncertain significance NCBI36 chr15: 29,852,369-100,338,915 , GRCh37.p13 chr15: 32,065,077-102,521,392 , GRCh38.p12 chr15: 31,772,874-101,981,189 GCHFR, SPPL2A, 1382 more genes
    nsv3920633copy number variation1nstd102humanPathogenic GRCh38 chr15: 68,830,574-73,823,337 , NCBI36 chr15: 66,909,967-71,902,731 , GRCh37 chr15: 69,122,913-74,115,678 NEO1, LOC390600, 95 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 RNU6-18P, GOLGA8K, 1442 more genes
    nsv3918770copy number variation1nstd102humanUncertain significance NCBI36 chr15: 20,280,728-100,338,915 , GRCh37.p13 chr15: 22,729,364-102,521,392 , GRCh38.p12 chr15: 23,319,714-101,981,189 SNRPCP18, SNORD116-30, 1622 more genes
    nsv3918644copy number variation1nstd102humanUncertain significance NCBI36 chr15: 20,313,935-100,338,915 , GRCh37.p13 chr15: 22,762,571-102,521,392 , GRCh38.p12 chr15: 23,319,714-101,981,189 SNORD116-23, UBE2Q2P6, 1622 more genes
    nsv3917589copy number variation1nstd102humanPathogenic GRCh37 chr15: 60,120,659-102,461,201 , GRCh38 chr15: 59,828,460-101,920,998 , NCBI36 chr15: 57,907,951-100,278,724 GAPDHP61, SNORD18B, 840 more genes
    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 H3P40, EEF1B2P1, 1616 more genes
    nsv3915210copy number variation1nstd102humanUncertain significance NCBI36 chr15: 28,207,117-100,338,915 , GRCh37.p13 chr15: 30,419,825-102,521,392 , GRCh38.p12 chr15: 30,127,622-101,981,189 RPL21P113, LOC112268152, 1428 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 SNX33, RNA5SP399, 209 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 MIR4513, LOC727751, 1754 more genes
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