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Items: 1 to 20 of 170

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5980459insertion1nstd102humanLikely benign GRCh38 chr1: 32,276,423-32,276,423 , GRCh37 chr1: 32,742,024-32,742,024 LCK
    nsv5676556mobile element insertion1nstd211human GRCh38 chr1: 32,262,848-32,262,848 , GRCh37.p13 chr1: 32,728,449-32,728,449 LCK
    nsv5615873insertion1nstd207human GRCh38 chr1: 32,266,691-32,266,691 , GRCh37.p13 chr1: 32,732,292-32,732,292 LCK
    nsv5552124insertion1nstd206human GRCh38 chr1: 32,284,200-32,284,250 , GRCh37.p13 chr1: 32,749,801-32,749,851 LCK
    nsv5420680copy number variation1nstd206human GRCh38 chr1: 32,268,222-32,269,786 , GRCh37.p13 chr1: 32,733,823-32,735,387 LCK
    nsv5419380copy number variation1nstd206human GRCh38 chr1: 32,261,464-32,261,770 , GRCh37.p13 chr1: 32,727,065-32,727,371 LCK
    nsv5204078copy number variation1nstd204human GRCh38.p13 chr1: 32,278,431-32,280,467 , GRCh37.p13 chr1: 32,744,032-32,746,068 LCK
    nsv5079885mobile element insertion1nstd203human GRCh38 chr1: 32,282,754-32,282,762 , GRCh37.p13 chr1: 32,748,355-32,748,363 LCK
    nsv5064897mobile element insertion1nstd203human GRCh38 chr1: 32,258,616-32,258,645 , GRCh37.p13 chr1: 32,724,217-32,724,246 LCK
    nsv4903324copy number variation1nstd200human GRCh38 chr1: 32,262,239-32,263,635 , GRCh37.p13 chr1: 32,727,840-32,729,236 LCK
    nsv4895817copy number variation1nstd200human GRCh38 chr1: 32,277,690-32,278,973 , GRCh37.p13 chr1: 32,743,291-32,744,574 LCK
    nsv4895816copy number variation1nstd200human GRCh38 chr1: 32,269,201-32,271,414 , GRCh37.p13 chr1: 32,734,802-32,737,015 LCK
    nsv4895815copy number variation1nstd200human GRCh38 chr1: 32,265,827-32,266,618 , GRCh37.p13 chr1: 32,731,428-32,732,219 LCK
    nsv4895814copy number variation1nstd200human GRCh38 chr1: 32,262,635-32,270,515 , GRCh37.p13 chr1: 32,728,236-32,736,116 LCK
    nsv4895813copy number variation1nstd200human GRCh38 chr1: 32,261,757-32,268,902 , GRCh37.p13 chr1: 32,727,358-32,734,503 LCK
    nsv4780757copy number variation1nstd200human GRCh37 chr1: 32,727,840-32,729,236 , GRCh38.p12 chr1: 32,262,239-32,263,635 LCK
    nsv4772966copy number variation1nstd200human GRCh37 chr1: 32,733,674-32,734,359 , GRCh38.p12 chr1: 32,268,073-32,268,758 LCK
    nsv4772965copy number variation1nstd200human GRCh37 chr1: 32,728,750-32,729,072 , GRCh38.p12 chr1: 32,263,149-32,263,471 LCK
    nsv4772964copy number variation1nstd200human GRCh37 chr1: 32,727,366-32,734,503 , GRCh38.p12 chr1: 32,261,765-32,268,902 LCK
    nsv4767860inversion1nstd199human GRCh37 chr1: 17,051,740-234,912,187 , GRCh38.p12 chr1: 16,725,245-234,776,440 , ABCA4, 4269 more genes
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