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Items: 1 to 20 of 147

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7076302inversion1nstd229human GRCh38 chr14: 46,512,743-51,785,975 , GRCh37.p13 chr14: 46,981,946-52,252,693 LOC100420098, MAP4K5, 82 more genes
    nsv7063700inversion1nstd229human GRCh38 chr14: 48,591,726-55,698,685 , GRCh37.p13 chr14: 49,060,929-56,165,403 ZFP64P1, LINC02331, 132 more genes
    nsv7059291inversion1nstd229human GRCh38 chr14: 49,838,942-56,572,993 , GRCh37.p13 chr14: 50,305,660-57,039,711 LOC105370500, LINC01599, 124 more genes
    nsv6949862copy number variation1nstd229human GRCh38 chr14: 51,123,112-56,995,885 , GRCh37.p13 chr14: 51,589,830-57,462,603 RPL3P3, RNA5SP385, 96 more genes
    nsv6943210copy number variation1nstd229human GRCh38 chr14: 51,131,026-51,657,439 , GRCh37.p13 chr14: 51,597,744-52,124,157 SETP2, RNU6-1291P, 8 more genes
    nsv6939197copy number variation1nstd229human GRCh38 chr14: 51,251,732-51,251,990 , GRCh37.p13 chr14: 51,718,450-51,718,708 TMX1
    nsv6938412copy number variation1nstd229human GRCh38 chr14: 46,367,427-52,468,480 , GRCh37.p13 chr14: 46,836,630-52,935,198 RNU6-297P, RN7SL452P, 95 more genes
    nsv6578746inversion1nstd223human GRCh38 chr14: 49,838,941-56,572,992 , GRCh37.p13 chr14: 50,305,659-57,039,710 LOC100419913, TXNDC16, 124 more genes
    nsv6315524copy number variation1nstd102humanPathogenic GRCh37 chr14: 37,671,058-106,985,955 , GRCh38.p12 chr14: 37,201,853-106,530,013 PAPOLA-DT, LOC105378180, 1338 more genes
    nsv6258859mobile element insertion1nstd215human GRCh38 chr14: 51,252,282-51,252,282 , GRCh37.p13 chr14: 51,719,000-51,719,000 TMX1
    nsv6199450copy number variation1nstd214human GRCh38 chr14: 51,238,709-51,238,762 , GRCh37.p13 chr14: 51,705,427-51,705,480 TMX1
    nsv6132787copy number variation1nstd213human GRCh37 chr14: 51,700,000-51,800,001 , GRCh38.p12 chr14: 51,233,282-51,333,283 TMX1, LINC00519, 2 more genes
    nsv6084344insertion1nstd212human GRCh38 chr14: 51,252,268-51,252,268 , GRCh37.p13 chr14: 51,718,986-51,718,986 TMX1
    nsv6040205copy number variation1nstd212human GRCh38 chr14: 51,238,724-51,238,778 , GRCh37.p13 chr14: 51,705,442-51,705,496 TMX1
    nsv5969788insertion1nstd209human GRCh38 chr14: 51,252,268-51,252,268 , GRCh37.p13 chr14: 51,718,986-51,718,986 TMX1
    nsv5941384copy number variation1nstd209human GRCh38 chr14: 51,238,709-51,238,762 , GRCh37.p13 chr14: 51,705,427-51,705,480 TMX1
    nsv5938835copy number variation1nstd209human GRCh38 chr14: 50,842,894-59,394,609 , GRCh37.p13 chr14: 51,309,612-59,861,327 , TMX1, 148 more genes
    nsv5935089copy number variation1nstd209human GRCh38 chr14: 46,941,699-52,127,962 , GRCh37.p13 chr14: 47,410,902-52,594,680 , RNA5SP385, 92 more genes
    nsv5695212mobile element insertion2nstd211human GRCh38 chr14: 51,252,282-51,252,282 , GRCh37.p13 chr14: 51,719,000-51,719,000 TMX1
    nsv5648696insertion1nstd207human GRCh38 chr14: 51,252,268-51,252,268 , GRCh37.p13 chr14: 51,718,986-51,718,986 TMX1
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