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Items: 1 to 20 of 273

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5723394mobile element insertion1nstd211human GRCh38 chr17: 75,722,045-75,722,045 , GRCh37.p13 chr17: 73,718,125-73,718,125 ITGB4
    nsv5717548mobile element insertion1nstd211human GRCh38 chr17: 75,722,058-75,722,058 , GRCh37.p13 chr17: 73,718,138-73,718,138 ITGB4
    nsv5560137mobile element insertion1nstd206human GRCh38 chr17: 75,722,058-75,722,102 , GRCh37.p13 chr17: 73,718,138-73,718,182 ITGB4
    nsv5518769copy number variation1nstd206human GRCh38 chr17: 75,748,100-75,748,409 , GRCh37.p13 chr17: 73,744,181-73,744,490 ITGB4
    nsv5349671translocation1nstd200human GRCh38 chr17: 75,738,655-75,738,655 , GRCh38 chr17: 75,738,601-75,738,601 , GRCh37.p13 chr17: 73,734,682-73,734,682 , GRCh37.p13 chr17: 73,734,736-73,734,736 ITGB4
    nsv5349670translocation1nstd200human GRCh38 chr17: 75,735,119-75,735,119 , GRCh38 chr17: 75,734,570-75,734,570 , GRCh37.p13 chr17: 73,730,651-73,730,651 , GRCh37.p13 chr17: 73,731,200-73,731,200 ITGB4
    nsv5330130translocation1nstd200human GRCh37 chr17: 73,734,682-73,734,682 , GRCh37 chr17: 73,734,736-73,734,736 , GRCh38.p12 chr17: 75,738,601-75,738,601 , GRCh38.p12 chr17: 75,738,655-75,738,655 ITGB4
    nsv5293343copy number variation1nstd204human GRCh38.p13 chr17: 74,899,101-76,684,700 , GRCh37.p13 chr17: 72,895,199-74,680,782 , RNU6-24P, 92 more genes
    nsv5282319copy number variation1nstd204human GRCh38.p13 chr17: 75,609,901-75,917,300 , GRCh37.p13 chr17: 73,605,982-73,913,381 ITGB4, TRIM65, 15 more genes
    nsv5143473mobile element insertion1nstd203human GRCh38 chr17: 75,735,711-75,735,726 , GRCh37.p13 chr17: 73,731,792-73,731,807 ITGB4
    nsv5142007mobile element insertion1nstd203human GRCh38 chr17: 75,726,689-75,726,725 , GRCh37.p13 chr17: 73,722,769-73,722,805 ITGB4
    nsv5016707copy number variation1nstd200human GRCh38 chr17: 75,749,320-75,749,429 , GRCh37.p13 chr17: 73,745,401-73,745,510 ITGB4
    nsv5016706copy number variation1nstd200human GRCh38 chr17: 75,723,416-75,726,611 , GRCh37.p13 chr17: 73,719,496-73,722,691 ITGB4
    nsv4685762copy number variation1nstd102humanPathogenic GRCh37 chr17: 73,735,514-73,739,660 , GRCh38.p12 chr17: 75,739,433-75,743,579 ITGB4
    nsv4676104copy number variation1nstd102humanPathogenic GRCh37 chr17: 73,261,871-78,608,763 , GRCh38.p12 chr17: 75,265,790-80,634,963 LLGL2, TSEN54, 165 more genes
    nsv4628995copy number variation1nstd183human GRCh37 chr17: 73,217,773-73,774,243 , GRCh38.p12 chr17: 75,221,678-75,778,162 , LOC107985013, 23 more genes
    nsv4569850inversion1nstd166human GRCh37.p13 chr17: 73,573,022-73,825,589 , GRCh38.p12 chr17: 75,576,941-75,829,508 GALK1, H3-3B, 10 more genes
    nsv4457679copy number variation1nstd102humanUncertain significance GRCh37 chr17: 73,596,063-73,959,466 , GRCh38.p12 chr17: 75,599,982-75,963,385 MIR4738, RECQL5, 16 more genes
    nsv4457646copy number variation1nstd102humanPathogenic GRCh37 chr17: 62,778,720-81,041,938 , GRCh38.p12 chr17: 64,782,602-83,084,062 LOC107985089, ARSG, 448 more genes
    nsv4416041copy number variation1nstd174human GRCh37 chr17: 73,717,370-73,737,100 , GRCh38.p12 chr17: 75,721,290-75,741,019 ITGB4
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