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Items: 1 to 20 of 81

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4544794insertion1nstd166human GRCh37.p13 chr19: 57,321,895-57,321,895 , GRCh38.p12 chr19: 56,810,527-56,810,527 PEG3, ZIM2, 1 more genes
    nsv4436360complex substitution1nstd102humanUncertain significance GRCh38.p12 chr19: 55,621,933-57,136,909 , GRCh37 chr19: 56,133,299-57,648,277 PEG3, U2AF2, 64 more genes
    nsv3962906copy number variation1nstd168human GRCh38 chr19: 56,803,464-56,813,881 , GRCh37.p13 chr19: 57,314,832-57,325,249 PEG3, PEG3-AS1, 1 more genes
    nsv3924732copy number variation1nstd102humanPathogenic GRCh38 chr19: 49,907,832-58,557,889 , GRCh37 chr19: 50,411,089-59,069,256 , NCBI36 chr19: 55,102,901-63,761,068 RPL39P37, CCDC106, 556 more genes
    nsv3923909copy number variation1nstd102humanPathogenic NCBI36 chr19: 55,347,589-63,784,382 , GRCh37 chr19: 50,655,777-59,092,570 , GRCh38 chr19: 50,152,520-58,581,203 OSCAR, FKBP1AP1, 535 more genes
    nsv3923613copy number variation1nstd102humanPathogenic GRCh38 chr19: 52,612,432-58,581,203 , GRCh37 chr19: 53,115,685-59,092,570 , NCBI36 chr19: 57,807,497-63,784,382 ZNF71-SMIM17, MIR518E, 393 more genes
    nsv3922599copy number variation1nstd102humanPathogenic GRCh38 chr19: 51,141,518-58,539,965 , NCBI36 chr19: 56,336,587-63,743,144 , GRCh37 chr19: 51,644,775-59,051,332 LOC100421130, A1BG-AS1, 475 more genes
    nsv3919766copy number variation1nstd102humanPathogenic NCBI36 chr19: 58,150,121-63,784,382 , GRCh37 chr19: 53,458,309-59,092,570 , GRCh38 chr19: 52,955,056-58,581,203 MIR520F, A1BG-AS1, 382 more genes
    nsv3919076copy number variation1nstd102humanPathogenic GRCh37 chr19: 48,432,832-59,083,573 , NCBI36 chr19: 53,124,644-63,775,385 , GRCh38 chr19: 47,929,575-58,572,206 KCNA7, ZNF28, 697 more genes
    nsv3917934copy number variation1nstd102humanLikely pathogenic NCBI36 chr19: 60,754,117-62,234,756 , GRCh37 chr19: 56,062,305-57,542,944 , GRCh38 chr19: 55,550,939-57,031,576 PEG3, U2AF2, 63 more genes
    nsv3916611copy number variation1nstd102humanPathogenic GRCh37 chr19: 50,694,476-59,047,185 , NCBI36 chr19: 55,386,288-63,738,997 , GRCh38 chr19: 50,191,219-58,535,818 RNU6-980P, ERVV-1, 526 more genes
    nsv3916295copy number variation1nstd102humanPathogenic NCBI36 chr19: 61,566,389-63,784,382 , GRCh37 chr19: 56,874,577-59,092,570 , GRCh38 chr19: 56,363,208-58,581,203 ZIM2, LOC100419848, 131 more genes
    nsv3914640copy number variation1nstd102humanUncertain significance NCBI36 chr19: 60,240,326-62,185,213 , GRCh37 chr19: 55,548,514-57,493,401 , GRCh38 chr19: 55,037,146-56,982,033 U2AF2, MIR7975, 101 more genes
    nsv3914098copy number variation1nstd102humanLikely pathogenic NCBI36 chr19: 60,251,694-62,175,638 , GRCh37 chr19: 55,595,687-57,483,826 , GRCh38 chr19: 55,048,514-56,972,458 IL11, PEG3, 99 more genes
    nsv3913991copy number variation1nstd102humanPathogenic NCBI36 chr19: 57,338,938-63,648,700 , GRCh37 chr19: 52,647,126-58,956,888 , GRCh38 chr19: 52,143,873-58,445,521 PEG3, ZNF480, 398 more genes
    nsv3912907copy number variation1nstd102humanUncertain significance GRCh38 chr19: 56,353,449-58,445,521 , NCBI36 chr19: 61,556,630-63,648,700 , GRCh37 chr19: 56,864,818-58,956,888 MIR4754, ZNF460-AS1, 114 more genes
    nsv3911950copy number variation1nstd102humanPathogenic GRCh37 chr19: 48,411,797-59,051,332 , NCBI36 chr19: 53,103,609-63,743,144 , GRCh38 chr19: 47,908,540-58,539,965 LOC107987270, MIR6799, 694 more genes
    nsv3905935copy number variation1nstd102humanUncertain significance GRCh37 chr19: 55,844,155-57,408,007 , GRCh38.p12 chr19: 55,332,787-56,896,639 ZSCAN5DP, ZNF524, 82 more genes
    nsv3904885copy number variation1nstd102humanPathogenic GRCh37 chr19: 68,029-59,110,290 , GRCh38.p12 chr19: 68,029-58,598,923 ZNF321P, ZNF861P, 2443 more genes
    nsv3904800copy number variation1nstd102humanUncertain significance GRCh37 chr19: 56,565,455-57,401,997 , GRCh38.p12 chr19: 56,054,089-56,890,629 NLRP5, ZNF471, 41 more genes
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