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Items: 1 to 20 of 1011

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6127297copy number variation1nstd186human GRCh37 chr18: 12,587,344-12,587,553 , GRCh38.p12 chr18: 12,587,345-12,587,554 SPIRE1
    nsv5978016insertion1nstd209human GRCh38 chr18: 12,491,252-12,491,252 , GRCh37.p13 chr18: 12,491,251-12,491,251 SPIRE1
    nsv5974664insertion1nstd209human GRCh38 chr18: 12,549,427-12,549,427 , GRCh37.p13 chr18: 12,549,426-12,549,426 SPIRE1
    nsv5946384copy number variation1nstd209human GRCh38 chr18: 12,654,125-12,654,896 , GRCh37.p13 chr18: 12,654,124-12,654,895 SPIRE1
    nsv5941324copy number variation1nstd209human GRCh38 chr18: 12,616,890-12,617,189 , GRCh37.p13 chr18: 12,616,889-12,617,188 SPIRE1
    nsv5938178copy number variation1nstd209human GRCh38 chr18: 12,503,664-12,504,385 , GRCh37.p13 chr18: 12,503,663-12,504,384 SPIRE1
    nsv5938025copy number variation1nstd209human GRCh38 chr18: 12,651,403-12,654,372 , GRCh37.p13 chr18: 12,651,402-12,654,371 SPIRE1
    nsv5933041copy number variation1nstd209human GRCh38 chr18: 12,587,345-12,587,538 , GRCh37.p13 chr18: 12,587,344-12,587,537 SPIRE1
    nsv5880204copy number variation1nstd209human GRCh38 chr18: 12,661,177-12,663,676 , GRCh37.p13 chr18: 12,661,176-12,663,675 PSMG2, SPIRE1, 1 more genes
    nsv5879588copy number variation1nstd209human GRCh38 chr18: 12,651,435-12,654,764 , GRCh37.p13 chr18: 12,651,434-12,654,763 SPIRE1
    nsv5728410mobile element insertion1nstd211human GRCh38 chr18: 12,455,966-12,455,966 , GRCh37.p13 chr18: 12,455,965-12,455,965 SPIRE1
    nsv5725961mobile element insertion2nstd211human GRCh38 chr18: 12,484,463-12,484,463 , GRCh37.p13 chr18: 12,484,462-12,484,462 SPIRE1
    nsv5712243mobile element insertion1nstd211human GRCh38 chr18: 12,631,206-12,631,206 , GRCh37.p13 chr18: 12,631,205-12,631,205 SPIRE1
    nsv5711353mobile element insertion2nstd211human GRCh38 chr18: 12,615,789-12,615,789 , GRCh37.p13 chr18: 12,615,788-12,615,788 SPIRE1
    nsv5704507mobile element insertion1nstd211human GRCh38 chr18: 12,583,022-12,583,022 , GRCh37.p13 chr18: 12,583,021-12,583,021 SPIRE1
    nsv5703703mobile element insertion1nstd211human GRCh38 chr18: 12,583,031-12,583,031 , GRCh37.p13 chr18: 12,583,030-12,583,030 SPIRE1
    nsv5703007mobile element insertion2nstd211human GRCh38 chr18: 12,452,232-12,452,232 , GRCh37.p13 chr18: 12,452,231-12,452,231 SPIRE1
    nsv5672896copy number variation1nstd102humanPathogenic GRCh37 chr18: 2,656,075-13,885,536 , GRCh38.p12 chr18: 2,656,076-13,885,537 RN7SL862P, LOC105371972, 181 more genes
    nsv5662223insertion1nstd207human GRCh38 chr18: 12,491,252-12,491,252 , GRCh37.p13 chr18: 12,491,251-12,491,251 SPIRE1
    nsv5647599insertion1nstd207human GRCh38 chr18: 12,596,875-12,596,875 , GRCh37.p13 chr18: 12,596,874-12,596,874 SPIRE1
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