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Items: 1 to 20 of 138

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5874499copy number variation1nstd209human GRCh38 chr2: 73,275,857-73,276,886 , GRCh37.p13 chr2: 73,502,985-73,504,014 FBXO41
    nsv5874145copy number variation1nstd209human GRCh38 chr2: 73,266,954-73,267,064 , GRCh37.p13 chr2: 73,494,082-73,494,192 FBXO41
    nsv5564339copy number variation1nstd102humanUncertain significance GRCh37 chr2: 73,114,549-73,836,749 , GRCh38.p12 chr2: 72,887,420-73,609,622 LOC105374800, SFXN5, 19 more genes
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5441491copy number variation1nstd206human GRCh38 chr2: 73,266,961-73,267,065 , GRCh37.p13 chr2: 73,494,089-73,494,193 FBXO41
    nsv5435877copy number variation1nstd206human GRCh38 chr2: 73,275,859-73,276,887 , GRCh37.p13 chr2: 73,502,987-73,504,015 FBXO41
    nsv5360784translocation1nstd200human GRCh38 chr2: 73,276,887-73,276,887 , GRCh38 chr2: 73,275,859-73,275,859 , GRCh37.p13 chr2: 73,502,987-73,502,987 , GRCh37.p13 chr2: 73,504,015-73,504,015 FBXO41
    nsv5339215translocation1nstd200human GRCh37 chr2: 73,502,987-73,502,987 , GRCh37 chr2: 73,504,015-73,504,015 , GRCh38.p12 chr2: 73,275,859-73,275,859 , GRCh38.p12 chr2: 73,276,887-73,276,887 FBXO41
    nsv5292310copy number variation1nstd204human GRCh38.p13 chr2: 73,275,835-73,276,916 , GRCh37.p13 chr2: 73,502,963-73,504,044 FBXO41
    nsv4731953copy number variation1nstd199human GRCh37 chr2: 73,503,694-73,503,751 , GRCh38.p12 chr2: 73,276,566-73,276,623 FBXO41
    nsv4658399copy number variation1nstd186human GRCh37 chr2: 73,502,985-73,504,015 , GRCh38.p12 chr2: 73,275,857-73,276,887 FBXO41
    nsv4586525copy number variation1nstd183human GRCh37 chr2: 73,502,985-73,504,015 , GRCh38.p12 chr2: 73,275,857-73,276,887 FBXO41
    nsv4394477copy number variation1nstd174human GRCh37 chr2: 73,502,954-73,504,031 , GRCh38.p12 chr2: 73,275,826-73,276,903 FBXO41
    nsv4067847copy number variation1nstd166human GRCh37.p13 chr2: 73,502,985-73,504,015 , GRCh38.p12 chr2: 73,275,857-73,276,887 FBXO41
    nsv4067654copy number variation1nstd166human GRCh37.p13 chr2: 73,512,063-73,524,815 , GRCh38.p12 chr2: 73,284,935-73,297,687 EGR4, RNU6-111P, 1 more genes
    nsv3916821copy number variation1nstd102humanPathogenic NCBI36 chr2: 47,701,031-86,783,356 , GRCh37.p13 chr2: 47,847,527-86,929,845 , GRCh38.p12 chr2: 47,620,388-86,702,722 NAGK, NRXN1-DT, 595 more genes
    nsv3910630copy number variation1nstd102humanPathogenic NCBI36 chr2: 50,739,936-242,751,149 , GRCh37.p13 chr2: 50,886,432-243,102,476 , GRCh38.p12 chr2: 50,659,294-242,160,331 DAZAP2P1, RPL36AP16, 2991 more genes
    nsv3903805copy number variation1nstd102humanBenign GRCh37 chr2: 7,635,254-88,005,418 , NCBI36 chr2: 7,552,705-87,786,533 , GRCh38 chr2: 7,495,123-87,705,899 LOC101927723, SANBR, 1246 more genes
    nsv3900298copy number variation1nstd102humanPathogenic GRCh37 chr2: 58,506,654-83,814,086 , GRCh38 chr2: 58,279,519-83,586,962 , NCBI36 chr2: 58,360,158-83,667,597 MIR1285-2, SERTAD2, 404 more genes
    nsv3885544copy number variation1nstd102humanPathogenic GRCh37 chr2: 14,238-243,048,760 , GRCh38.p12 chr2: 14,238-242,106,609 RNU6-674P, KANSL3, 3735 more genes
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