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Items: 1 to 20 of 205

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095479copy number variation1nstd102humanUncertain significance GRCh37 chr19: 38,375,572-39,738,787 , GRCh38.p12 chr19: 37,884,932-39,248,147 HNRNPL, RN7SL663P, 45 more genes
    nsv7068075inversion1nstd229human GRCh38 chr19: 38,271,689-38,284,176 , GRCh37.p13 chr19: 38,762,329-38,774,816 SPINT2
    nsv7066225inversion1nstd229human GRCh38 chr19: 38,205,926-38,272,809 , GRCh37.p13 chr19: 38,696,566-38,763,449 SPINT2, SIPA1L3, 2 more genes
    nsv7012575copy number variation1nstd229human GRCh38 chr19: 38,260,418-38,263,835 , GRCh37.p13 chr19: 38,751,058-38,754,475 SPINT2
    nsv7008156copy number variation1nstd229human GRCh38 chr19: 36,851,242-46,031,790 , GRCh37.p13 chr19: 37,342,144-46,535,048 LOC105372390, LOC107985291, 396 more genes
    nsv7005713copy number variation1nstd229human GRCh38 chr19: 33,458,650-39,721,746 , GRCh37.p13 chr19: 33,949,556-40,212,386 , TYROBP, 259 more genes
    nsv6599662inversion1nstd223human GRCh38 chr19: 38,286,763-38,287,294 , GRCh37.p13 chr19: 38,777,403-38,777,934 SPINT2
    nsv6598682inversion1nstd223human GRCh38 chr19: 38,262,366-38,262,791 , GRCh37.p13 chr19: 38,753,006-38,753,431 SPINT2
    nsv6528802copy number variation1nstd223human GRCh38 chr19: 37,602,649-38,484,499 , GRCh37.p13 chr19: 38,093,550-38,975,139 SPRED3, PSMD8, 30 more genes
    nsv6515767copy number variation1nstd223human GRCh38 chr19: 38,276,054-38,323,179 , GRCh37.p13 chr19: 38,766,694-38,813,819 YIF1B, KCNK6, 2 more genes
    nsv6290300copy number variation1nstd102humanPathogenic GRCh37 chr19: 19,546,923-41,313,229 , GRCh38.p12 chr19: 19,436,114-40,807,324 ZNF420, LOC105372330, 574 more genes
    nsv6229188insertion1nstd214human GRCh38 chr19: 38,269,831-38,269,831 , GRCh37.p13 chr19: 38,760,471-38,760,471 SPINT2
    nsv6133523copy number variation1nstd213human GRCh37 chr19: 34,000,000-42,200,001 , GRCh38.p12 chr19: 33,509,094-41,696,083 , ACTN4, 345 more genes
    nsv6130240insertion1nstd186human GRCh37 chr19: 38,760,419-38,760,456 , GRCh38.p12 chr19: 38,269,779-38,269,816 SPINT2
    nsv6107601insertion1nstd212human GRCh38 chr19: 38,269,930-38,269,930 , GRCh37.p13 chr19: 38,760,570-38,760,570 SPINT2
    nsv6106785insertion1nstd212human GRCh38 chr19: 38,275,337-38,275,337 , GRCh37.p13 chr19: 38,765,977-38,765,977 SPINT2
    nsv6101388insertion1nstd212human GRCh38 chr19: 38,279,497-38,279,497 , GRCh37.p13 chr19: 38,770,137-38,770,137 SPINT2
    nsv5942667copy number variation1nstd209human GRCh38 chr19: 38,276,604-38,286,744 , GRCh37.p13 chr19: 38,767,244-38,777,384 SPINT2
    nsv5883235copy number variation1nstd209human GRCh38 chr19: 38,276,589-38,285,449 , GRCh37.p13 chr19: 38,767,229-38,776,089 SPINT2
    nsv5646749insertion1nstd207human GRCh38 chr19: 38,269,831-38,269,831 , GRCh37.p13 chr19: 38,760,471-38,760,471 SPINT2
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