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Items: 1 to 20 of 173

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5978275inversion1nstd209human GRCh38 chr20: 49,834,476-49,834,735 , GRCh37.p13 chr20: 48,451,013-48,451,272 SLC9A8
    nsv5721725mobile element insertion1nstd211human GRCh38 chr20: 49,852,818-49,852,818 , GRCh37.p13 chr20: 48,469,355-48,469,355 SLC9A8
    nsv5666153insertion1nstd207human GRCh38 chr20: 49,834,375-49,834,375 , GRCh37.p13 chr20: 48,450,912-48,450,912 SLC9A8
    nsv5603483copy number variation1nstd207human GRCh38 chr20: 49,834,352-49,834,432 , GRCh37.p13 chr20: 48,450,889-48,450,969 SLC9A8
    nsv5602254copy number variation1nstd207human GRCh38 chr20: 49,884,227-49,884,278 , GRCh37.p13 chr20: 48,500,764-48,500,815 SLC9A8
    nsv5560525inversion1nstd206human GRCh38 chr20: 49,834,386-49,834,451 , GRCh37.p13 chr20: 48,450,923-48,450,988 SLC9A8
    nsv5554434mobile element insertion1nstd206human GRCh38 chr20: 49,852,818-49,852,869 , GRCh37.p13 chr20: 48,469,355-48,469,406 SLC9A8
    nsv5526766copy number variation1nstd206human GRCh38 chr20: 49,610,386-49,857,118 , GRCh37.p13 chr20: 48,226,923-48,473,655 B4GALT5, SLC9A8, 6 more genes
    nsv5521126copy number variation1nstd206human GRCh38 chr20: 49,811,122-49,811,356 , GRCh37.p13 chr20: 48,427,659-48,427,893 SLC9A8
    nsv5366149translocation1nstd200human GRCh38 chr20: 49,834,300-49,834,300 , GRCh38 chr20: 49,827,334-49,827,334 , GRCh37.p13 chr20: 48,450,837-48,450,837 , GRCh37.p13 chr20: 48,443,871-48,443,871 SLC9A8, RNU7-72P, 1 more genes
    nsv5361916translocation1nstd200human GRCh38 chr20: 49,814,046-49,814,046 , GRCh38 chr3: 128,953,441-128,953,441 , GRCh37.p13 chr20: 48,430,583-48,430,583 , GRCh37.p13 chr3: 128,672,284-128,672,284 CFAP92, SLC9A8
    nsv5337288translocation1nstd200human GRCh37 chr20: 48,430,583-48,430,583 , GRCh37 chr3: 128,672,284-128,672,284 , GRCh38.p12 chr20: 49,814,046-49,814,046 , GRCh38.p12 chr3: 128,953,441-128,953,441 SLC9A8, CFAP92
    nsv5337140translocation1nstd200human GRCh37 chr20: 48,494,853-48,494,853 , GRCh37 chr3: 48,252,129-48,252,129 , GRCh38.p12 chr3: 48,210,639-48,210,639 , GRCh38.p12 chr20: 49,878,316-49,878,316 SLC9A8
    nsv5195612mobile element insertion1nstd203human GRCh38 chr20: 49,852,804-49,852,818 , GRCh37.p13 chr20: 48,469,341-48,469,355 SLC9A8
    nsv5189482mobile element insertion1nstd203human GRCh38 chr20: 49,852,808-49,852,818 , GRCh37.p13 chr20: 48,469,345-48,469,355 SLC9A8
    nsv5180298mobile element insertion1nstd203human GRCh38 chr20: 49,847,926-49,847,936 , GRCh37.p13 chr20: 48,464,463-48,464,473 SLC9A8
    nsv5012998copy number variation1nstd200human GRCh38 chr20: 49,837,314-49,839,379 , GRCh37.p13 chr20: 48,453,851-48,455,916 SLC9A8
    nsv4853782copy number variation1nstd200human GRCh37 chr20: 48,429,799-48,433,663 , GRCh38.p12 chr20: 49,813,262-49,817,126 SLC9A8
    nsv4746913copy number variation1nstd199human GRCh37 chr20: 48,450,854-48,450,928 , GRCh38.p12 chr20: 49,834,317-49,834,391 SLC9A8
    nsv4722639mobile element insertion1nstd186human GRCh37 chr20: 48,469,341-48,469,341 , GRCh38.p12 chr20: 49,852,804-49,852,804 SLC9A8
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