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Items: 1 to 20 of 135

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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
    nsv7066225inversion1nstd229human GRCh38 chr19: 38,205,926-38,272,809 , GRCh37.p13 chr19: 38,696,566-38,763,449 SPINT2, SIPA1L3, 2 more genes
    nsv7064025inversion1nstd229human GRCh38 chr19: 38,253,139-38,253,228 , GRCh37.p13 chr19: 38,743,779-38,743,868 PPP1R14A
    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
    nsv6999039copy number variation1nstd229human GRCh38 chr19: 38,242,122-38,251,451 , GRCh37.p13 chr19: 38,732,762-38,742,091 PPP1R14A
    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
    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
    nsv6133523copy number variation1nstd213human GRCh37 chr19: 34,000,000-42,200,001 , GRCh38.p12 chr19: 33,509,094-41,696,083 , ACTN4, 345 more genes
    nsv5876486copy number variation1nstd209human GRCh38 chr19: 38,237,515-38,256,977 , GRCh37.p13 chr19: 38,728,155-38,747,617 PPP1R14A
    nsv5292599copy number variation1nstd204human GRCh38.p13 chr19: 38,256,865-38,258,864 , GRCh37.p13 chr19: 38,747,505-38,749,504 PPP1R14A
    nsv5160377mobile element insertion1nstd203human GRCh38 chr19: 38,250,092-38,250,092 , GRCh37.p13 chr19: 38,740,732-38,740,732 PPP1R14A
    nsv5024613copy number variation1nstd200human GRCh38 chr19: 38,232,450-38,271,814 , GRCh37.p13 chr19: 38,723,090-38,762,454 SPINT2, PPP1R14A
    nsv4865155copy number variation1nstd200human GRCh37 chr19: 38,723,090-38,762,454 , GRCh38.p12 chr19: 38,232,450-38,271,814 PPP1R14A, SPINT2
    nsv4679943copy number variation1nstd189human GRCh37.p13 chr19: 37,838,926-38,764,481 , GRCh38.p12 chr19: 37,348,024-38,273,841 DPF1, SPINT2, 31 more genes
    nsv4676223copy number variation1nstd102humanUncertain significance GRCh37 chr19: 38,512,717-39,291,526 , GRCh38.p12 chr19: 38,022,077-38,800,886 MAP4K1-AS1, LGALS7B, 25 more genes
    nsv4457372copy number variation1nstd102humanPathogenic GRCh37 chr19: 28,271,106-49,213,832 , GRCh38.p12 chr19: 27,780,198-48,710,575 ZNF461, LOC101927572, 735 more genes
    nsv4265019copy number variation1nstd166human GRCh37.p13 chr19: 38,729,000-38,748,000 , GRCh38.p12 chr19: 38,238,360-38,257,360 PPP1R14A
    nsv4257924copy number variation1nstd166human GRCh37.p13 chr19: 38,717,338-38,761,436 , GRCh38.p12 chr19: 38,226,698-38,270,796 DPF1, SPINT2, 1 more genes
    nsv3913730copy number variation1nstd102humanPathogenic NCBI36 chr19: 11,199,618-49,821,491 , GRCh37 chr19: 11,338,618-45,129,651 , GRCh38 chr19: 11,227,942-44,626,354 BCKDHA, ADGRE5, 1102 more genes
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