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Items: 1 to 20 of 217

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4431049copy number variation1nstd174human GRCh37 chr19: 53,346,827-53,480,869 , GRCh38.p12 chr19: 52,843,574-52,977,616 ZNF816, ZNF468, 5 more genes
    nsv4420773copy number variation1nstd174human GRCh37 chr19: 53,112,568-53,552,217 , GRCh38.p12 chr19: 52,609,315-53,048,964 ZNF816, ZNF701, 18 more genes
    nsv4359761copy number variation1nstd102humanPathogenic NCBI36 chr19: 53,124,644-63,775,385 , GRCh37.p13 chr19: 48,432,832-59,083,573 , GRCh38.p12 chr19: 47,929,575-58,572,206 ZNF816, AP2A1, 706 more genes
    nsv4359567copy number variation1nstd102humanPathogenic NCBI36 chr19: 57,807,497-63,784,382 , GRCh37.p13 chr19: 53,115,685-59,092,570 , GRCh38.p12 chr19: 52,612,432-58,581,203 ZNF816, A1BG, 399 more genes
    nsv4358385copy number variation1nstd102humanPathogenic NCBI36 chr19: 55,102,901-63,761,068 , GRCh37.p13 chr19: 50,411,089-59,069,256 , GRCh38.p12 chr19: 49,907,832-58,557,889 ZNF816, A1BG, 563 more genes
    nsv4356651copy number variation1nstd102humanPathogenic NCBI36 chr19: 58,150,121-63,784,382 , GRCh37.p13 chr19: 53,458,309-59,092,570 , GRCh38.p12 chr19: 52,955,056-58,581,203 ZNF816, FCAR, 387 more genes
    nsv4355461copy number variation1nstd102humanUncertain significance NCBI36 chr19: 57,902,300-58,387,693 , GRCh37.p13 chr19: 53,210,488-53,695,881 , GRCh38.p12 chr19: 52,707,235-53,192,628 ZNF816, ZNF600, 20 more genes
    nsv4355384copy number variation1nstd102humanPathogenic NCBI36 chr19: 53,103,609-63,743,144 , GRCh37.p13 chr19: 48,411,797-59,051,332 , GRCh38.p12 chr19: 47,908,540-58,539,965 ZNF816, AP2A1, 703 more genes
    nsv4352365copy number variation1nstd102humanPathogenic NCBI36 chr19: 55,386,288-63,738,997 , GRCh37.p13 chr19: 50,694,476-59,047,185 , GRCh38.p12 chr19: 50,191,219-58,535,818 ZNF816, A1BG, 533 more genes
    nsv4352290copy number variation1nstd102humanPathogenic NCBI36 chr19: 56,336,587-63,743,144 , GRCh37.p13 chr19: 51,644,775-59,051,332 , GRCh38.p12 chr19: 51,141,518-58,539,965 ZNF816, FCAR, 481 more genes
    nsv4351845copy number variation1nstd102humanPathogenic NCBI36 chr19: 55,347,589-63,784,382 , GRCh37.p13 chr19: 50,655,777-59,092,570 , GRCh38.p12 chr19: 50,152,520-58,581,203 ZNF816, KLK3, 542 more genes
    nsv4350033copy number variation1nstd102humanUncertain significance GRCh37 chr19: 53,119,399-53,432,969 , GRCh38.p12 chr19: 52,616,146-52,929,716 ZNF28, ZNF468, 11 more genes
    nsv4349056copy number variation1nstd102humanPathogenic GRCh37 chr19: 52,647,126-58,956,888 , GRCh38.p12 chr19: 52,143,873-58,445,521 ZNF816, A1BG, 403 more genes
    nsv4339133sequence alteration1nstd166human GRCh37.p13 chr19: 53,193,026-53,869,624 , GRCh38.p12 chr19: 52,689,773-53,366,371 ZNF816, ZNF28, 35 more genes
    nsv4312559insertion1nstd166human GRCh37.p13 chr19: 44,160,393-53,443,548 , GRCh38.p12 chr19: 43,656,241-52,940,295 AP2A1, APOC4, 511 more genes
    nsv4272099copy number variation1nstd166human GRCh37.p13 chr19: 53,459,474-53,462,161 , GRCh38.p12 chr19: 52,956,221-52,958,908 ZNF816, ZNF816-ZNF321P
    nsv4271922copy number variation1nstd166human GRCh37.p13 chr19: 53,424,000-53,430,000 , GRCh38.p12 chr19: 52,920,747-52,926,747 ZNF888, ZNF321P, 1 more genes
    nsv4271224copy number variation1nstd166human GRCh37.p13 chr19: 53,428,802-53,429,963 , GRCh38.p12 chr19: 52,925,549-52,926,710 ZNF816-ZNF321P, ZNF888, 1 more genes
    nsv4269642copy number variation1nstd166human GRCh37.p13 chr19: 53,102,912-53,449,557 , GRCh38.p12 chr19: 52,599,659-52,946,304 ZNF701, ZNF83, 12 more genes
    nsv4269236copy number variation1nstd166human GRCh37.p13 chr19: 53,431,577-53,442,512 , GRCh38.p12 chr19: 52,928,324-52,939,259 ZNF888, ZNF321P, 1 more genes
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