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Items: 1 to 20 of 170

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5935517copy number variation1nstd209human GRCh38 chr15: 74,723,439-74,758,382 , GRCh37.p13 chr15: 75,015,780-75,050,723 CYP1A1, CYP1A2
    nsv5933606copy number variation1nstd209human GRCh38 chr15: 71,577,714-80,433,232 , GRCh37.p13 chr15: 71,870,053-80,725,573 , STRA6, 229 more genes
    nsv5864012copy number variation1nstd209human GRCh38 chr15: 74,740,067-74,753,686 , GRCh37.p13 chr15: 75,032,408-75,046,027 CYP1A2
    nsv5849430copy number variation1nstd209human GRCh38 chr15: 74,756,167-74,758,566 , GRCh37.p13 chr15: 75,048,508-75,050,907 CYP1A2
    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
    nsv4992346copy number variation1nstd200human GRCh38 chr15: 74,755,547-74,756,173 , GRCh37.p13 chr15: 75,047,888-75,048,514 CYP1A2
    nsv4992345copy number variation1nstd200human GRCh38 chr15: 74,723,443-74,758,383 , GRCh37.p13 chr15: 75,015,784-75,050,724 CYP1A1, CYP1A2
    nsv4992298copy number variation1nstd200human GRCh38 chr15: 73,152,590-82,101,178 , GRCh37.p13 chr15: 73,444,931-82,393,519 , SNUPN, 215 more genes
    nsv4850095copy number variation1nstd200human GRCh37 chr15: 75,015,784-75,050,724 , GRCh38.p12 chr15: 74,723,443-74,758,383 CYP1A2, CYP1A1
    nsv4729106copy number variation1nstd102humanPathogenic GRCh37 chr15: 74,398,162-76,054,094 , GRCh38.p12 chr15: 74,105,821-75,761,753 FAM219B, MIR4513, 62 more genes
    nsv4675298copy number variation1nstd102humanUncertain significance GRCh37 chr15: 75,039,267-75,268,029 , GRCh38.p12 chr15: 74,746,926-74,975,688 SCAMP2, CSK, 11 more genes
    nsv4455940copy number variation1nstd102humanPathogenic GRCh37 chr15: 72,943,184-75,544,524 , GRCh38.p12 chr15: 72,650,843-75,252,183 TBC1D21, CPLX3, 72 more genes
    nsv4455912copy number variation1nstd102humanPathogenic GRCh37 chr15: 72,963,271-76,064,900 , GRCh38.p12 chr15: 72,670,930-75,772,559 MIR6881, ARID3B, 94 more genes
    nsv4455687copy number variation1nstd102humanPathogenic GRCh37 chr15: 72,926,922-75,544,524 , GRCh38.p12 chr15: 72,634,581-75,252,183 SCAMP2, LOC105376731, 74 more genes
    nsv4369169copy number variation1nstd173human GRCh37 chr15: 75,012,579-75,040,420 , GRCh38.p12 chr15: 74,720,238-74,748,079 CYP1A2, CYP1A1
    nsv4244008copy number variation1nstd166human GRCh37.p13 chr15: 75,048,134-75,053,234 , GRCh38.p12 chr15: 74,755,793-74,760,893 CYP1A2
    nsv4240616copy number variation1nstd166human GRCh37.p13 chr15: 75,015,784-75,050,724 , GRCh38.p12 chr15: 74,723,443-74,758,383 CYP1A2, CYP1A1
    nsv3970728copy number variation1nstd168human GRCh38 chr15: 74,748,501-74,767,475 , GRCh37.p13 chr15: 75,040,842-75,059,816 CYP1A2
    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
    nsv3920789copy number variation1nstd102humanLikely pathogenic NCBI36 chr15: 70,751,023-73,279,197 , GRCh37 chr15: 72,963,970-75,492,144 , GRCh38 chr15: 72,671,629-75,199,803 BBS4, CLK3, 67 more genes
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