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Items: 1 to 20 of 143

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5919138copy number variation1nstd209human GRCh38 chr10: 52,766,742-52,769,473 , GRCh37.p13 chr10: 54,526,502-54,529,233 MBL2
    nsv5865248copy number variation1nstd209human GRCh38 chr10: 52,766,775-52,769,512 , GRCh37.p13 chr10: 54,526,535-54,529,272 MBL2
    nsv5489716copy number variation1nstd206human GRCh38 chr10: 52,766,743-52,769,474 , GRCh37.p13 chr10: 54,526,503-54,529,234 MBL2
    nsv5485569copy number variation1nstd206human GRCh38 chr10: 52,553,169-52,835,728 , GRCh37.p13 chr10: 54,312,929-54,595,488 LOC105378306, MBL2, 2 more genes
    nsv5483967copy number variation1nstd206human GRCh38 chr10: 52,764,459-52,774,001 , GRCh37.p13 chr10: 54,524,219-54,533,761 MBL2
    nsv5380868copy number variation1nstd102humanUncertain significance GRCh37 chr10: 54,011,320-54,530,789 , GRCh38.p12 chr10: 52,251,560-52,771,029 RPL31P44, DKK1, 6 more genes
    nsv5347677translocation1nstd200human GRCh38 chr10: 52,764,459-52,764,459 , GRCh38 chr10: 52,774,001-52,774,001 , GRCh37.p13 chr10: 54,524,219-54,524,219 , GRCh37.p13 chr10: 54,533,761-54,533,761 MBL2
    nsv5316299copy number variation1nstd204human GRCh38.p13 chr10: 52,766,740-52,769,483 , GRCh37.p13 chr10: 54,526,500-54,529,243 MBL2
    nsv5253286copy number variation1nstd204human GRCh38.p13 chr10: 52,765,975-52,769,512 , GRCh37.p13 chr10: 54,525,735-54,529,272 MBL2
    nsv5033632inversion1nstd200human GRCh38 chr10: 36,819,152-58,318,428 , GRCh37.p13 chr10: 37,108,080-60,078,188 , LOC107001062, 306 more genes
    nsv4970008copy number variation1nstd200human GRCh38 chr10: 52,766,743-52,769,474 , GRCh37.p13 chr10: 54,526,503-54,529,234 MBL2
    nsv4870857inversion1nstd200human GRCh37 chr10: 37,108,081-60,078,188 , GRCh38.p12 chr10: 36,819,153-58,318,428 , NCOA4, 306 more genes
    nsv4835935copy number variation1nstd200human GRCh37 chr10: 54,526,503-54,529,234 , GRCh38.p12 chr10: 52,766,743-52,769,474 MBL2
    nsv4675455copy number variation1nstd102humanPathogenic GRCh37 chr10: 50,250,603-69,256,083 , GRCh38.p12 chr10: 45,931,517-67,496,325 MRLN, LOC102724778, 242 more genes
    nsv4675213copy number variation1nstd102humanUncertain significance GRCh37 chr10: 53,802,602-55,217,542 , GRCh38.p12 chr10: 52,042,842-53,457,782 DKK1, RPL31P44, 13 more genes
    nsv4672687copy number variation1nstd186human GRCh37 chr10: 54,526,502-54,529,234 , GRCh38.p12 chr10: 52,766,742-52,769,474 MBL2
    nsv4667055copy number variation1nstd186human GRCh37 chr10: 54,526,625-54,529,250 , GRCh38.p12 chr10: 52,766,865-52,769,490 MBL2
    nsv4617862copy number variation1nstd183human GRCh37 chr10: 54,526,628-54,529,238 , GRCh38.p12 chr10: 52,766,868-52,769,478 MBL2
    nsv4611607copy number variation1nstd183human GRCh37 chr10: 54,526,625-54,529,250 , GRCh38.p12 chr10: 52,766,865-52,769,490 MBL2
    nsv4609520copy number variation1nstd183human GRCh37 chr10: 54,500,931-57,442,625 , GRCh38.p12 chr10: 52,741,171-55,682,865 LOC105378307, NEFMP1, 14 more genes
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