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Items: 1 to 20 of 441

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6126563copy number variation1nstd186human GRCh37 chr17: 27,126,380-27,127,183 , GRCh38.p12 chr17: 28,799,362-28,800,165 FAM222B
    nsv5970482insertion1nstd209human GRCh38 chr17: 28,790,884-28,790,884 , GRCh37.p13 chr17: 27,117,902-27,117,902 FAM222B
    nsv5945665copy number variation1nstd209human GRCh38 chr17: 28,829,152-28,829,419 , GRCh37.p13 chr17: 27,156,170-27,156,437 FAM222B
    nsv5945123copy number variation1nstd209human GRCh38 chr17: 28,847,070-28,853,039 , GRCh37.p13 chr17: 27,174,088-27,180,057 ERAL1, FAM222B
    nsv5941389copy number variation1nstd209human GRCh38 chr17: 28,799,392-28,800,125 , GRCh37.p13 chr17: 27,126,410-27,127,143 FAM222B
    nsv5939530copy number variation1nstd209human GRCh38 chr17: 28,779,618-28,811,311 , GRCh37.p13 chr17: 27,106,636-27,138,329 FAM222B, RPL31P58
    nsv5939244copy number variation1nstd209human GRCh38 chr17: 28,783,757-28,784,045 , GRCh37.p13 chr17: 27,110,775-27,111,063 FAM222B
    nsv5936762copy number variation1nstd209human GRCh38 chr17: 28,798,864-28,799,219 , GRCh37.p13 chr17: 27,125,882-27,126,237 FAM222B
    nsv5936310copy number variation1nstd209human GRCh38 chr17: 28,846,616-28,852,602 , GRCh37.p13 chr17: 27,173,634-27,179,620 FAM222B
    nsv5885622copy number variation1nstd209human GRCh38 chr17: 28,801,994-28,808,766 , GRCh37.p13 chr17: 27,129,012-27,135,784 FAM222B, RPL31P58
    nsv5884219copy number variation2nstd209human GRCh38 chr17: 28,847,836-28,852,543 , GRCh37.p13 chr17: 27,174,854-27,179,561 FAM222B
    nsv5880201copy number variation1nstd209human GRCh38 chr17: 28,789,236-28,800,625 , GRCh37.p13 chr17: 27,116,254-27,127,643 FAM222B, RPL31P58
    nsv5878910copy number variation1nstd209human GRCh38 chr17: 28,755,346-28,763,013 , GRCh37.p13 chr17: 27,082,364-27,090,031 FAM222B
    nsv5874668copy number variation1nstd209human GRCh38 chr17: 28,795,702-28,797,225 , GRCh37.p13 chr17: 27,122,720-27,124,243 FAM222B
    nsv5873249copy number variation1nstd209human GRCh38 chr17: 28,820,999-28,822,198 , GRCh37.p13 chr17: 27,148,017-27,149,216 FAM222B
    nsv5870108copy number variation2nstd209human GRCh38 chr17: 28,794,064-28,795,101 , GRCh37.p13 chr17: 27,121,082-27,122,119 FAM222B
    nsv5720745mobile element insertion1nstd211human GRCh38 chr17: 28,826,384-28,826,384 , GRCh37.p13 chr17: 27,153,402-27,153,402 FAM222B
    nsv5712812mobile element insertion1nstd211human GRCh38 chr17: 28,789,103-28,789,103 , GRCh37.p13 chr17: 27,116,121-27,116,121 FAM222B
    nsv5712732mobile element insertion1nstd211human GRCh38 chr17: 28,822,865-28,822,865 , GRCh37.p13 chr17: 27,149,883-27,149,883 FAM222B
    nsv5706135mobile element insertion1nstd211human GRCh38 chr17: 28,793,278-28,793,278 , GRCh37.p13 chr17: 27,120,296-27,120,296 FAM222B
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