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Items: 1 to 20 of 114

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5935349copy number variation1nstd209human GRCh38 chr15: 77,970,674-82,312,707 , GRCh37.p13 chr15: 78,263,016-82,605,043 , ST20, 91 more genes
    nsv5933606copy number variation1nstd209human GRCh38 chr15: 71,577,714-80,433,232 , GRCh37.p13 chr15: 71,870,053-80,725,573 , STRA6, 229 more genes
    nsv5556515sequence alteration1nstd206human GRCh38 chr15: 77,975,462-78,778,174 , GRCh37.p13 chr15: 78,267,804-79,070,516 , CHRNA5, 26 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
    nsv5151032mobile element insertion1nstd203human GRCh38 chr15: 78,339,270-78,339,285 , GRCh37.p13 chr15: 78,631,612-78,631,627 CRABP1
    nsv4992298copy number variation1nstd200human GRCh38 chr15: 73,152,590-82,101,178 , GRCh37.p13 chr15: 73,444,931-82,393,519 , SNUPN, 215 more genes
    nsv4621307copy number variation1nstd183human GRCh37 chr15: 78,553,094-78,744,929 , GRCh38.p12 chr15: 78,260,752-78,452,587 CRABP1, IREB2, 6 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
    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
    nsv3919138copy number variation1nstd102humanUncertain significance GRCh38 chr15: 77,640,317-78,459,174 , GRCh37 chr15: 77,932,659-78,751,516 , NCBI36 chr15: 75,719,714-76,538,571 IDH3A, CRABP1, 21 more genes
    nsv3918992copy number variation1nstd102humanPathogenic NCBI36 chr15: 75,141,730-95,931,047 , GRCh37.p13 chr15: 77,354,675-98,130,043 , GRCh38.p12 chr15: 77,062,333-97,586,813 TLNRD1, FES, 403 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
    nsv3918013copy number variation1nstd102humanLikely benign NCBI36 chr15: 76,278,105-76,992,310 , GRCh38 chr15: 78,198,708-78,912,913 , GRCh37 chr15: 78,491,050-79,205,255 PSMA4, LOC646934, 24 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
    nsv3915187copy number variation1nstd102humanPathogenic NCBI36 chr15: 70,234,344-100,278,724 , GRCh37 chr15: 72,447,290-102,461,201 , GRCh38 chr15: 72,154,949-101,920,998 LOC102724117, TMEM266, 618 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
    nsv3913830copy number variation1nstd102humanPathogenic GRCh38 chr15: 76,006,154-79,982,417 , NCBI36 chr15: 74,085,550-78,061,814 , GRCh37 chr15: 76,298,495-80,274,759 TSPAN3, LOC105370919, 86 more genes
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