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Items: 1 to 20 of 123

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148115copy number variation1nstd102humanUncertain significance GRCh37 chr15: 49,775,348-51,221,365 , GRCh38.p12 chr15: 49,483,151-50,929,168 RNA5SP395, AHCYP7, 24 more genes
    nsv7067502inversion1nstd229human GRCh38 chr15: 48,513,881-51,354,383 , GRCh37.p13 chr15: 48,806,078-51,646,580 NDUFAF4P1, MIR4713, 49 more genes
    nsv6967925copy number variation1nstd229human GRCh38 chr15: 49,880,745-49,881,079 , GRCh37.p13 chr15: 50,172,942-50,173,276 ATP8B4, LOC102724587
    nsv6637384copy number variation1nstd102humanPathogenic GRCh37 chr15: 48,589,845-63,543,438 , GRCh38.p12 chr15: 48,297,648-63,251,239 LINC03065, FAM227B, 228 more genes
    nsv6505107copy number variation1nstd223human GRCh38 chr15: 49,880,745-49,881,079 , GRCh37.p13 chr15: 50,172,942-50,173,276 LOC102724587, ATP8B4
    nsv6313917copy number variation1nstd102humanPathogenic GRCh37 chr15: 47,635,238-56,509,908 , GRCh38.p12 chr15: 47,343,041-56,217,710 PYGO1, RNU6-449P, 125 more genes
    nsv6307312copy number variation1nstd186human GRCh37 chr15: 50,172,959-50,173,281 , GRCh38.p12 chr15: 49,880,762-49,881,084 ATP8B4, LOC102724587
    nsv6144695copy number variation1nstd206human GRCh38 chr15: 49,880,762-49,881,084 , GRCh37.p13 chr15: 50,172,959-50,173,281 ATP8B4, LOC102724587
    nsv6132897copy number variation1nstd213human GRCh37 chr15: 50,000,000-53,730,001 , GRCh38.p12 chr15: 49,707,803-53,437,804 MAPK6, ARPP19, 65 more genes
    nsv5945785copy number variation1nstd209human GRCh38 chr15: 49,880,094-49,906,469 , GRCh37.p13 chr15: 50,172,291-50,198,666 LOC102724587, ATP8B4
    nsv5861883copy number variation1nstd209human GRCh38 chr15: 49,880,053-49,906,471 , GRCh37.p13 chr15: 50,172,250-50,198,668 ATP8B4, LOC102724587
    nsv5389783copy number variation2nstd186human GRCh37 chr15: 50,172,942-50,173,281 , GRCh38.p12 chr15: 49,880,745-49,881,084 ATP8B4, LOC102724587
    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
    nsv5318366copy number variation1nstd204human GRCh38.p13 chr15: 49,880,739-49,881,089 , GRCh37.p13 chr15: 50,172,936-50,173,286 LOC102724587, ATP8B4
    nsv5038422inversion1nstd200human GRCh38 chr15: 40,121,948-64,050,807 , GRCh37.p13 chr15: 40,414,149-64,343,006 , EIF4EBP2P2, 475 more genes
    nsv5005379copy number variation1nstd200human GRCh38 chr15: 49,880,745-49,881,084 , GRCh37.p13 chr15: 50,172,942-50,173,281 ATP8B4, LOC102724587
    nsv4872280inversion1nstd200human GRCh37 chr15: 40,414,149-64,343,008 , GRCh38.p12 chr15: 40,121,948-64,050,809 , DNAAF4-CCPG1, 475 more genes
    nsv4863780copy number variation1nstd200human GRCh37 chr15: 50,172,942-50,173,281 , GRCh38.p12 chr15: 49,880,745-49,881,084 LOC102724587, ATP8B4
    nsv4769387copy number variation1nstd102humanPathogenic GRCh37 chr15: 48,744,917-53,851,050 , GRCh38.p12 chr15: 48,452,720-53,558,853 BCL2L10, RNA5SP394, 86 more genes
    nsv4675095copy number variation1nstd102humanPathogenic GRCh37 chr15: 47,192,561-50,819,726 , GRCh38.p12 chr15: 46,900,363-50,527,529 LOC102724587, LOC645405, 51 more genes
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