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Items: 1 to 20 of 350

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5955309copy number variation1nstd209human GRCh38 chr22: 37,730,894-37,732,460 , GRCh37.p13 chr22: 38,126,901-38,128,467 TRIOBP
    nsv5954488copy number variation1nstd209human GRCh38 chr22: 37,705,037-37,705,338 , GRCh37.p13 chr22: 38,101,044-38,101,345 TRIOBP
    nsv5711023mobile element insertion1nstd211human GRCh38 chr22: 37,760,285-37,760,285 , GRCh37.p13 chr22: 38,156,292-38,156,292 TRIOBP
    nsv5699383mobile element insertion1nstd211human GRCh38 chr22: 37,740,567-37,740,567 , GRCh37.p13 chr22: 38,136,574-38,136,574 TRIOBP
    nsv5698807mobile element insertion2nstd211human GRCh38 chr22: 37,738,880-37,738,880 , GRCh37.p13 chr22: 38,134,887-38,134,887 TRIOBP
    nsv5665287insertion1nstd207human GRCh38 chr22: 37,724,034-37,724,034 , GRCh37.p13 chr22: 38,120,041-38,120,041 TRIOBP
    nsv5552564copy number variation1nstd206human GRCh38 chr22: 37,736,684-37,741,331 , GRCh37.p13 chr22: 38,132,691-38,137,338 TRIOBP
    nsv5550047copy number variation1nstd206human GRCh38 chr22: 37,694,031-37,695,069 , GRCh37.p13 chr22: 38,090,038-38,091,076 TRIOBP
    nsv5542582copy number variation1nstd206human GRCh38 chr22: 37,730,916-37,732,516 , GRCh37.p13 chr22: 38,126,923-38,128,523 TRIOBP
    nsv5540611copy number variation1nstd206human GRCh38 chr22: 37,758,009-37,758,064 , GRCh37.p13 chr22: 38,154,016-38,154,071 TRIOBP
    nsv5538329copy number variation1nstd206human GRCh38 chr22: 37,730,655-37,734,253 , GRCh37.p13 chr22: 38,126,662-38,130,260 TRIOBP
    nsv5536753copy number variation1nstd206human GRCh38 chr22: 37,723,638-37,724,497 , GRCh37.p13 chr22: 38,119,645-38,120,504 TRIOBP
    nsv5432089mobile element insertion1nstd206human GRCh38 chr22: 37,738,880-37,738,931 , GRCh37.p13 chr22: 38,134,887-38,134,938 TRIOBP
    nsv5426260mobile element insertion1nstd206human GRCh38 chr22: 37,740,567-37,740,618 , GRCh37.p13 chr22: 38,136,574-38,136,625 TRIOBP
    nsv5414242mobile element insertion1nstd206human GRCh38 chr22: 37,760,285-37,760,336 , GRCh37.p13 chr22: 38,156,292-38,156,343 TRIOBP
    nsv5360565translocation1nstd200human GRCh38 chr22: 37,736,684-37,736,684 , GRCh38 chr22: 37,741,331-37,741,331 , GRCh37.p13 chr22: 38,137,338-38,137,338 , GRCh37.p13 chr22: 38,132,691-38,132,691 TRIOBP
    nsv5360564translocation1nstd200human GRCh38 chr22: 37,720,520-37,720,520 , GRCh38 chr22: 37,720,602-37,720,602 , GRCh37.p13 chr22: 38,116,527-38,116,527 , GRCh37.p13 chr22: 38,116,609-38,116,609 TRIOBP
    nsv5321633copy number variation1nstd204human GRCh38.p13 chr22: 37,694,026-37,695,176 , GRCh37.p13 chr22: 38,090,033-38,091,183 TRIOBP
    nsv5281012copy number variation1nstd204human GRCh38.p13 chr22: 37,662,501-37,724,300 , GRCh37.p13 chr22: 38,058,508-38,120,307 LGALS1, PDXP, 3 more genes
    nsv5200376copy number variation1nstd102humanPathogenic GRCh37 chr22: 38,155,164-38,541,997 , GRCh38.p12 chr22: 37,759,157-38,145,990 H1-0, PLA2G6, 18 more genes
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