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Items: 1 to 20 of 228

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5948843insertion1nstd209human GRCh38 chr10: 95,256,977-95,256,977 , GRCh37.p13 chr10: 97,016,734-97,016,734 PDLIM1
    nsv5921993copy number variation1nstd209human GRCh38 chr10: 90,979,234-99,692,336 , GRCh37.p13 chr10: 92,738,991-101,452,093 , CYP2C115P, 166 more genes
    nsv5917786copy number variation1nstd209human GRCh38 chr10: 95,238,111-95,238,566 , GRCh37.p13 chr10: 96,997,868-96,998,323 PDLIM1
    nsv5915946copy number variation1nstd209human GRCh38 chr10: 95,238,684-95,247,212 , GRCh37.p13 chr10: 96,998,441-97,006,969 PDLIM1
    nsv5915043copy number variation1nstd209human GRCh38 chr10: 95,247,366-95,263,862 , GRCh37.p13 chr10: 97,007,123-97,023,619 PDLIM1
    nsv5911623copy number variation1nstd209human GRCh38 chr10: 95,265,869-95,266,164 , GRCh37.p13 chr10: 97,025,626-97,025,921 PDLIM1
    nsv5910099copy number variation1nstd209human GRCh38 chr10: 95,271,782-95,290,816 , GRCh37.p13 chr10: 97,031,539-97,050,573 PDLIM1
    nsv5710038mobile element insertion2nstd211human GRCh38 chr10: 95,274,085-95,274,085 , GRCh37.p13 chr10: 97,033,842-97,033,842 PDLIM1
    nsv5703904mobile element insertion1nstd211human GRCh38 chr10: 95,239,129-95,239,129 , GRCh37.p13 chr10: 96,998,886-96,998,886 PDLIM1
    nsv5546892insertion1nstd206human GRCh38 chr10: 95,239,129-95,239,180 , GRCh37.p13 chr10: 96,998,886-96,998,937 PDLIM1
    nsv5546857insertion1nstd206human GRCh38 chr10: 95,257,001-95,257,027 , GRCh37.p13 chr10: 97,016,758-97,016,784 PDLIM1
    nsv5404630mobile element insertion1nstd206human GRCh38 chr10: 95,274,085-95,274,136 , GRCh37.p13 chr10: 97,033,842-97,033,893 PDLIM1
    nsv5366664translocation1nstd200human GRCh38 chr2: 176,299,950-176,299,950 , GRCh38 chr10: 95,291,035-95,291,035 , GRCh37.p13 chr10: 97,050,792-97,050,792 , GRCh37.p13 chr2: 177,164,678-177,164,678 MTX2, PDLIM1
    nsv5330308translocation1nstd200human GRCh37 chr10: 97,050,792-97,050,792 , GRCh37 chr2: 177,164,678-177,164,678 , GRCh38.p12 chr10: 95,291,035-95,291,035 , GRCh38.p12 chr2: 176,299,950-176,299,950 PDLIM1, MTX2
    nsv5324620translocation1nstd204human GRCh37.p13 chr10: 97,050,791-97,050,791 , GRCh37.p13 chr2: 177,164,678-177,164,678 , GRCh38.p13 chr2: 176,299,950-176,299,950 , GRCh38.p13 chr10: 95,291,034-95,291,034 PDLIM1, MTX2
    nsv5121441mobile element insertion1nstd203human GRCh38 chr10: 95,274,069-95,274,085 , GRCh37.p13 chr10: 97,033,826-97,033,842 PDLIM1
    nsv4986788copy number variation1nstd200human GRCh38 chr10: 95,250,840-95,255,130 , GRCh37.p13 chr10: 97,010,597-97,014,887 PDLIM1
    nsv4729709copy number variation1nstd102humanUncertain significance GRCh37 chr10: 96,140,621-97,222,801 , GRCh38.p12 chr10: 94,380,864-95,463,044 LOC107984257, RPL7AP52, 18 more genes
    nsv4717207mobile element insertion1nstd186human GRCh37 chr10: 97,016,751-97,016,751 , GRCh38.p12 chr10: 95,256,994-95,256,994 PDLIM1
    nsv4670527copy number variation1nstd186human GRCh37 chr10: 96,856,006-97,066,884 , GRCh38.p12 chr10: 95,096,249-95,307,127 , PDLIM1, 3 more genes
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