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Items: 1 to 20 of 116

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5970408inversion1nstd209human GRCh38 chr19: 2,282,477-7,636,587 , GRCh37.p13 chr19: 2,282,476-7,701,473 , TLE5, 195 more genes
    nsv5967934inversion1nstd209human GRCh38 chr19: 5,658,814-5,764,360 , GRCh37.p13 chr19: 5,658,825-5,764,371 SAFB, LONP1, 5 more genes
    nsv5942775copy number variation1nstd209human GRCh38 chr19: 2,865,023-7,153,898 , GRCh37.p13 chr19: 2,865,021-7,153,909 , GNA15-DT, 159 more genes
    nsv5928846copy number variation1nstd209human GRCh38 chr19: 5,688,859-5,689,559 , GRCh37.p13 chr19: 5,688,870-5,689,570 RPL36, HSD11B1L
    nsv5556725sequence alteration1nstd206human GRCh38 chr19: 5,658,847-5,764,391 , GRCh37.p13 chr19: 5,658,858-5,764,402 SAFB, LONP1, 5 more genes
    nsv5546886insertion1nstd206human GRCh38 chr19: 5,684,673-5,684,688 , GRCh37.p13 chr19: 5,684,684-5,684,699 HSD11B1L
    nsv5523728copy number variation1nstd206human GRCh38 chr19: 5,688,839-5,689,580 , GRCh37.p13 chr19: 5,688,850-5,689,591 HSD11B1L, RPL36
    nsv5329085copy number variation1nstd204human GRCh37.p13 chr19: 5,688,866-5,689,540 , GRCh38.p13 chr19: 5,688,855-5,689,529 HSD11B1L, RPL36
    nsv5283595copy number variation1nstd204human GRCh38.p13 chr19: 5,683,801-5,761,700 , GRCh37.p13 chr19: 5,683,812-5,761,711 HSD11B1L, LONP1, 2 more genes
    nsv5027434copy number variation1nstd200human GRCh38 chr19: 5,688,105-5,688,822 , GRCh37.p13 chr19: 5,688,116-5,688,833 HSD11B1L, RPL36
    nsv5027432copy number variation1nstd200human GRCh38 chr19: 5,677,066-5,685,512 , GRCh37.p13 chr19: 5,677,077-5,685,523 HSD11B1L, MICOS13, 1 more genes
    nsv5014416copy number variation1nstd200human GRCh38 chr19: 5,519,830-5,914,524 , GRCh37.p13 chr19: 5,519,841-5,914,535 FUT5, CATSPERD, 19 more genes
    nsv4852735copy number variation1nstd200human GRCh37 chr19: 5,688,886-5,689,519 , GRCh38.p12 chr19: 5,688,875-5,689,508 RPL36, HSD11B1L
    nsv4627296copy number variation1nstd183human GRCh37 chr19: 5,685,090-5,685,311 , GRCh38.p12 chr19: 5,685,079-5,685,300 HSD11B1L
    nsv4624218copy number variation1nstd183human GRCh37 chr19: 5,685,090-5,685,135 , GRCh38.p12 chr19: 5,685,079-5,685,124 HSD11B1L
    nsv4621390copy number variation1nstd183human GRCh37 chr19: 5,681,099-5,685,135 , GRCh38.p12 chr19: 5,681,088-5,685,124 HSD11B1L, MICOS13
    nsv4545946insertion1nstd166human GRCh37.p13 chr19: 5,684,648-5,684,648 , GRCh38.p12 chr19: 5,684,637-5,684,637 HSD11B1L
    nsv4457772copy number variation1nstd102humanUncertain significance GRCh37 chr19: 5,513,058-5,776,260 , GRCh38.p12 chr19: 5,513,047-5,776,249 LONP1, RPL36, 8 more genes
    nsv4255820copy number variation1nstd166human GRCh37.p13 chr19: 5,661,195-5,741,612 , GRCh38.p12 chr19: 5,661,184-5,741,601 SAFB, LONP1, 5 more genes
    nsv3924480copy number variation1nstd102humanUncertain significance NCBI36 chr19: 5,401,983-6,486,595 , GRCh37.p13 chr19: 5,450,983-6,535,595 , GRCh38.p12 chr19: 5,450,972-6,535,584 TINCR, SAFB2, 42 more genes
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