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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3972399copy number variation1nstd102humanLikely pathogenic GRCh37 (hg19) chr17: 64,159,738-74,891,024 , GRCh38.p12 chr17: 66,163,620-76,894,942 , NCBI36 (hg18) chr17: 61,590,200-72,402,619 LLGL2, GALK1, 252 more genes
    nsv3931422copy number variation1nstd167human GRCh37 (hg19) chr17: 73,554,887-73,554,967 , GRCh38.p12 chr17: 75,558,806-75,558,886 LLGL2
    nsv3919156copy number variation1nstd102humanPathogenic GRCh38 (hg38) chr17: 69,916,435-83,102,552 , GRCh37.p13 chr17: 67,912,576-81,060,055 , NCBI36 (hg18) chr17: 65,424,171-78,653,717 LLGL2, AANAT, 381 more genes
    nsv3917654copy number variation1nstd102humanPathogenic GRCh38 (hg38) chr17: 69,209,079-83,086,677 , GRCh37.p13 chr17: 67,205,220-81,044,553 , NCBI36 (hg18) chr17: 64,716,815-78,637,842 LLGL2, BIRC5, 390 more genes
    nsv3914783copy number variation1nstd102humanPathogenic NCBI36 (hg18) chr17: 16,698,288-78,654,742 , GRCh37.p13 chr17: 16,757,563-81,048,189 , GRCh38.p12 chr17: 16,854,249-83,103,577 LLGL2, ASIC2, 1916 more genes
    nsv3911811copy number variation1nstd102humanPathogenic NCBI36 (hg18) chr17: 31,824,931-78,654,742 , GRCh37.p13 chr17: 34,750,818-81,048,189 , GRCh38.p12 chr17: 36,382,248-83,103,577 LLGL2, BIRC5, 1391 more genes
    nsv3909523copy number variation1nstd102humanPathogenic GRCh37 (hg19) chr17: 63,689,671-81,041,938 , GRCh38.p12 chr17: 65,693,553-83,084,062 , NCBI36 (hg18) chr17: 61,120,133-78,635,227 LLGL2, ACTG1, 452 more genes
    nsv3909511copy number variation1nstd102humanPathogenic GRCh37 (hg19) chr17: 42,580,684-81,085,615 , GRCh38.p12 chr17: 44,503,316-83,137,846 , NCBI36 (hg18) chr17: 39,936,210-78,641,478 LLGL2, ACOX1, 996 more genes
    nsv3907261copy number variation2nstd102humanPathogenic GRCh37 (hg19) chr17: 526-81,041,938 , GRCh38.p12 chr17: 150,733-83,084,062 , NCBI36 (hg18) chr17: 526-78,635,227 LLGL2, ACADVL, 2437 more genes
    nsv3906245copy number variation1nstd102humanPathogenic GRCh37 (hg19) chr17: 12,344-81,057,996 , GRCh38.p12 chr17: 162,553-83,100,251 , NCBI36 (hg18) chr17: 12,344-78,641,478 LLGL2, AANAT, 2438 more genes
    nsv3906075copy number variation1nstd102humanPathogenic GRCh37 (hg19) chr17: 67,002,415-81,041,938 , GRCh38.p12 chr17: 69,006,274-83,084,062 , NCBI36 (hg18) chr17: 64,514,010-78,635,227 LLGL2, AANAT, 396 more genes
    nsv3903684copy number variation1nstd102humanPathogenic GRCh37 (hg19) chr17: 8,547-81,060,040 , GRCh38.p12 chr17: 158,756-83,102,004 , NCBI36 (hg18) chr17: 8,547-78,641,478 LLGL2, ACADVL, 2438 more genes
    nsv3903313copy number variation1nstd102humanPathogenic GRCh37 (hg19) chr17: 64,241,326-81,041,938 , GRCh38.p12 chr17: 66,245,208-83,084,062 , NCBI36 (hg18) chr17: 61,671,788-78,635,227 LLGL2, AANAT, 446 more genes
    nsv3903198copy number variation1nstd102humanBenign GRCh37 (hg19) chr17: 73,517,536-73,544,160 , GRCh38.p12 chr17: 75,521,455-75,548,079 , NCBI36 (hg18) chr17: 71,029,131-71,055,755 LLGL2, TSEN54, 1 more genes
    nsv3899740copy number variation1nstd102humanPathogenic GRCh37 (hg19) chr17: 7,214-81,058,310 , GRCh38.p12 chr17: 157,423-83,100,564 , NCBI36 (hg18) chr17: 7,214-78,641,478 LLGL2, ADORA2B, 2438 more genes
    nsv3898032copy number variation1nstd102humanUncertain significance GRCh37 (hg19) chr17: 73,414,856-74,037,715 , GRCh38.p12 chr17: 75,418,775-76,041,634 , NCBI36 (hg18) chr17: 70,926,451-71,549,310 LLGL2, EVPL, 27 more genes
    nsv3897774copy number variation1nstd102humanBenign GRCh37 (hg19) chr17: 73,517,536-73,568,125 , GRCh38.p12 chr17: 75,521,455-75,572,044 , NCBI36 (hg18) chr17: 71,029,131-71,079,720 LLGL2, LOC107985023, 1 more genes
    nsv3897173copy number variation1nstd102humanBenign GRCh37 (hg19) chr17: 73,565,171-73,690,287 , GRCh38.p12 chr17: 75,569,090-75,694,207 , NCBI36 (hg18) chr17: 71,076,766-71,201,882 LLGL2, MYO15B, 5 more genes
    nsv3895416copy number variation1nstd102humanBenign GRCh37 (hg19) chr17: 73,542,671-73,543,084 , GRCh38.p12 chr17: 75,546,590-75,547,003 , NCBI36 (hg18) chr17: 71,054,266-71,054,679 LLGL2
    nsv3890986copy number variation1nstd102humanBenign GRCh37 (hg19) chr17: 73,517,536-73,627,539 , GRCh38.p12 chr17: 75,521,455-75,631,459 , NCBI36 (hg18) chr17: 71,029,131-71,139,134 LLGL2, RECQL5, 4 more genes
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