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Items: 1 to 20 of 113

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5723030mobile element insertion1nstd211human GRCh38 chr10: 72,942,520-72,942,520 , GRCh37.p13 chr10: 74,702,278-74,702,278 PLA2G12B
    nsv5555550mobile element insertion1nstd206human GRCh38 chr10: 72,942,520-72,942,571 , GRCh37.p13 chr10: 74,702,278-74,702,329 PLA2G12B
    nsv5486342copy number variation1nstd206human GRCh38 chr10: 72,948,314-72,952,543 , GRCh37.p13 chr10: 74,708,072-74,712,301 PLA2G12B
    nsv5485803copy number variation1nstd206human GRCh38 chr10: 72,943,063-72,949,184 , GRCh37.p13 chr10: 74,702,821-74,708,942 PLA2G12B
    nsv5347851translocation1nstd200human GRCh38 chr10: 72,943,063-72,943,063 , GRCh38 chr10: 72,949,183-72,949,183 , GRCh37.p13 chr10: 74,702,821-74,702,821 , GRCh37.p13 chr10: 74,708,941-74,708,941 PLA2G12B
    nsv5132077mobile element insertion1nstd203human GRCh38 chr10: 72,940,481-72,940,486 , GRCh37.p13 chr10: 74,700,239-74,700,244 PLA2G12B
    nsv5030933inversion1nstd200human GRCh38 chr10: 57,233,666-95,028,660 , GRCh37.p13 chr10: 58,993,426-96,788,417 , RNU6-740P, 615 more genes
    nsv4976516copy number variation1nstd200human GRCh38 chr10: 72,948,314-72,952,543 , GRCh37.p13 chr10: 74,708,072-74,712,301 PLA2G12B
    nsv4614181copy number variation1nstd183human GRCh37 chr10: 74,702,819-74,708,942 , GRCh38.p12 chr10: 72,943,061-72,949,184 PLA2G12B
    nsv4343722sequence alteration1nstd166human GRCh37.p13 chr10: 43,905,894-92,001,956 , GRCh38.p12 chr10: 43,410,446-90,242,199 , ALOX5, 749 more genes
    nsv4339713sequence alteration1nstd166human GRCh37.p13 chr10: 8,718,069-114,609,729 , GRCh38.p12 chr10: 8,676,106-112,849,970 , ADRA2A, 1651 more genes
    nsv4191903copy number variation1nstd166human GRCh37.p13 chr10: 74,702,821-74,708,942 , GRCh38.p12 chr10: 72,943,063-72,949,184 PLA2G12B
    nsv4182018copy number variation1nstd166human GRCh37.p13 chr10: 74,695,521-74,695,951 , GRCh38.p12 chr10: 72,935,763-72,936,193 PLA2G12B
    nsv3948483insertion1nstd167human GRCh37 chr10: 74,700,239-74,700,239 , GRCh38.p12 chr10: 72,940,481-72,940,481 PLA2G12B
    nsv3924859copy number variation1nstd102humanPathogenic NCBI36 chr10: 52,159,133-88,896,941 , GRCh38 chr10: 50,729,367-87,147,204 , GRCh37 chr10: 52,489,127-88,906,961 BMS1P4-AGAP5, MTCO2P23, 471 more genes
    nsv3922335copy number variation1nstd102humanPathogenic GRCh37 chr10: 60,196,226-76,174,974 , GRCh38 chr10: 58,436,466-74,415,216 , NCBI36 chr10: 59,866,232-75,844,980 UNC5B-AS1, ALDH7A1P4, 250 more genes
    nsv3917966copy number variation1nstd102humanPathogenic NCBI36 chr10: 68,626,331-80,851,819 , GRCh37 chr10: 68,956,325-81,181,813 , GRCh38 chr10: 67,196,567-79,422,057 LINC02640, HK1, 231 more genes
    nsv3917822copy number variation1nstd102humanPathogenic GRCh38 chr10: 63,402,579-75,296,099 , GRCh37 chr10: 65,162,339-77,055,857 , NCBI36 chr10: 64,832,345-76,725,863 MYL6P3, CHCHD1, 220 more genes
    nsv3917047copy number variation1nstd102humanPathogenic NCBI36 chr10: 42,500,760-75,145,672 , GRCh37 chr10: 43,180,754-75,475,666 , GRCh38 chr10: 42,685,306-73,715,908 SLC9A3P3, JMJD1C-AS2, 476 more genes
    nsv3910545copy number variation1nstd102humanPathogenic NCBI36 chr10: 74,150,392-77,042,138 , GRCh38 chr10: 72,720,628-75,612,374 , GRCh37 chr10: 74,480,386-77,372,132 CAMK2G, MCU, 73 more genes
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