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Items: 1 to 20 of 641

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5965417insertion1nstd209human GRCh38 chr5: 180,941,895-180,941,895 , GRCh37.p13 chr5: 180,368,895-180,368,895 BTNL8
    nsv5958334insertion1nstd209human GRCh38 chr5: 180,922,591-180,922,591 , GRCh37.p13 chr5: 180,349,591-180,349,591 BTNL8
    nsv5896132copy number variation1nstd209human GRCh38 chr5: 180,948,146-181,003,606 , GRCh37.p13 chr5: 180,375,146-180,430,606 BTNL3, BTNL8, 3 more genes
    nsv5842516copy number variation2nstd209human GRCh38 chr5: 180,942,295-180,943,294 , GRCh37.p13 chr5: 180,369,295-180,370,294 BTNL8
    nsv5842515copy number variation1nstd209human GRCh38 chr5: 180,882,945-180,923,265 , GRCh37.p13 chr5: 180,309,945-180,350,265 BTNL8
    nsv5842251copy number variation1nstd209human GRCh38 chr5: 180,909,489-180,929,369 , GRCh37.p13 chr5: 180,336,489-180,356,369 BTNL8
    nsv5842249copy number variation1nstd209human GRCh38 chr5: 180,853,070-180,902,121 , GRCh37.p13 chr5: 180,280,070-180,329,121 BTNL8, ZFP62
    nsv5841961copy number variation2nstd209human GRCh38 chr5: 180,949,226-180,965,880 , GRCh37.p13 chr5: 180,376,226-180,392,880 TMEM69P2, BTNL8, 1 more genes
    nsv5841960copy number variation1nstd209human GRCh38 chr5: 180,934,916-180,946,725 , GRCh37.p13 chr5: 180,361,916-180,373,725 BTNL8, RPS29P12
    nsv5716689mobile element insertion1nstd211human GRCh38 chr5: 180,902,189-180,902,189 , GRCh37.p13 chr5: 180,329,189-180,329,189 BTNL8
    nsv5693999mobile element insertion2nstd211human GRCh38 chr5: 180,941,914-180,941,914 , GRCh37.p13 chr5: 180,368,914-180,368,914 BTNL8
    nsv5693852mobile element insertion2nstd211human GRCh38 chr5: 180,922,604-180,922,604 , GRCh37.p13 chr5: 180,349,604-180,349,604 BTNL8
    nsv5690429mobile element insertion2nstd211human GRCh38 chr5: 180,914,694-180,914,694 , GRCh37.p13 chr5: 180,341,694-180,341,694 BTNL8
    nsv5642810insertion1nstd207human GRCh38 chr5: 180,917,113-180,917,113 , GRCh37.p13 chr5: 180,344,113-180,344,113 BTNL8
    nsv5642586insertion1nstd207human GRCh38 chr5: 180,941,895-180,941,895 , GRCh37.p13 chr5: 180,368,895-180,368,895 BTNL8
    nsv5640758insertion1nstd207human GRCh38 chr5: 180,917,440-180,917,440 , GRCh37.p13 chr5: 180,344,440-180,344,440 BTNL8
    nsv5635640insertion1nstd207human GRCh38 chr5: 180,922,591-180,922,591 , GRCh37.p13 chr5: 180,349,591-180,349,591 BTNL8
    nsv5580910copy number variation1nstd207human GRCh38 chr5: 180,948,027-181,003,527 , GRCh37.p13 chr5: 180,375,027-180,430,527 BTNL3, BTNL8, 3 more genes
    nsv5464234copy number variation1nstd206human GRCh38 chr5: 180,908,770-180,908,837 , GRCh37.p13 chr5: 180,335,770-180,335,837 BTNL8
    nsv5457522copy number variation1nstd206human GRCh38 chr5: 180,942,662-180,943,316 , GRCh37.p13 chr5: 180,369,662-180,370,316 BTNL8
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