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Items: 1 to 20 of 702

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6130456insertion1nstd186human GRCh37 chr18: 59,792,230-59,792,266 , GRCh38.p12 chr18: 62,124,997-62,125,033 PIGN
    nsv6128972copy number variation1nstd186human GRCh37 chr18: 59,769,698-59,769,781 , GRCh38.p12 chr18: 62,102,465-62,102,548 PIGN
    nsv6127621copy number variation1nstd186human GRCh37 chr18: 59,706,963-59,707,225 , GRCh38.p12 chr18: 62,039,730-62,039,992 PIGN
    nsv6114546mobile element insertion1nstd186human GRCh37 chr18: 59,713,719-59,713,719 , GRCh38.p12 chr18: 62,046,486-62,046,486 PIGN
    nsv6112815copy number variation1nstd102humanPathogenic GRCh37 chr18: 54,285,235-77,960,815 , GRCh38.p12 chr18: 56,618,004-80,202,932 RPL31P9, TRG-TCC5-1, 271 more genes
    nsv6112802copy number variation1nstd102humanPathogenic GRCh37 chr18: 23,626,739-78,014,976 , GRCh38.p12 chr18: 26,046,775-80,257,093 RPL9P31, LINC02582, 595 more genes
    nsv5977891insertion1nstd209human GRCh38 chr18: 62,062,882-62,062,882 , GRCh37.p13 chr18: 59,730,115-59,730,115 PIGN
    nsv5973434insertion1nstd209human GRCh38 chr18: 62,103,371-62,103,371 , GRCh37.p13 chr18: 59,770,604-59,770,604 PIGN
    nsv5971742insertion1nstd209human GRCh38 chr18: 62,046,486-62,046,486 , GRCh37.p13 chr18: 59,713,719-59,713,719 PIGN
    nsv5944787copy number variation1nstd209human GRCh38 chr18: 62,102,487-62,102,547 , GRCh37.p13 chr18: 59,769,720-59,769,780 PIGN
    nsv5941018copy number variation1nstd209human GRCh38 chr18: 62,138,261-62,140,520 , GRCh37.p13 chr18: 59,805,494-59,807,753 PIGN
    nsv5937981copy number variation1nstd209human GRCh38 chr18: 62,040,172-62,040,237 , GRCh37.p13 chr18: 59,707,405-59,707,470 PIGN
    nsv5727746mobile element insertion2nstd211human GRCh38 chr18: 62,103,385-62,103,385 , GRCh37.p13 chr18: 59,770,618-59,770,618 PIGN
    nsv5722469mobile element insertion1nstd211human GRCh38 chr18: 62,063,203-62,063,203 , GRCh37.p13 chr18: 59,730,436-59,730,436 PIGN
    nsv5718739mobile element insertion1nstd211human GRCh38 chr18: 62,071,278-62,071,278 , GRCh37.p13 chr18: 59,738,511-59,738,511 PIGN
    nsv5715970mobile element insertion2nstd211human GRCh38 chr18: 62,154,475-62,154,475 , GRCh37.p13 chr18: 59,821,708-59,821,708 PIGN
    nsv5714234mobile element insertion1nstd211human GRCh38 chr18: 62,107,116-62,107,116 , GRCh37.p13 chr18: 59,774,349-59,774,349 PIGN
    nsv5710375mobile element insertion2nstd211human GRCh38 chr18: 62,046,501-62,046,501 , GRCh37.p13 chr18: 59,713,734-59,713,734 PIGN
    nsv5695756mobile element insertion1nstd211human GRCh38 chr18: 62,095,752-62,095,752 , GRCh37.p13 chr18: 59,762,985-59,762,985 PIGN
    nsv5695478mobile element insertion1nstd211human GRCh38 chr18: 62,096,543-62,096,543 , GRCh37.p13 chr18: 59,763,776-59,763,776 PIGN
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