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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3169696copy number variation33nstd156human NCBI36 (hg18) chr11: 4,194,982-4,341,373 , GRCh38.p2 chr11: 4,217,176-4,363,567 , GRCh37.p13 chr11: 4,238,406-4,384,797 SSU72P3, SSU72P5, 4 more genes
    nsv3138161copy number variation1nstd151human GRCh37 (hg19) chr1: 1,452,544-1,509,942 , GRCh38 (hg38) chr1: 1,517,164-1,574,562 SSU72, ATAD3A, 1 more genes
    nsv3135882copy number variation1nstd151human GRCh37 (hg19) chr7: 123,593,622-124,537,232 , GRCh38 (hg38) chr7: 123,953,568-124,897,178 SPAM1, C7orf77, 12 more genes
    nsv3133486copy number variation1nstd151human GRCh37 (hg19) chr1: 1,421,157-1,565,089 , GRCh38 (hg38) chr1: 1,485,777-1,629,709 SSU72, MIB2, 6 more genes
    nsv3132736copy number variation1nstd151human GRCh37 (hg19) chr1: 1,454,298-1,670,501 , GRCh38 (hg38) chr1: 1,518,918-1,739,062 SSU72, MMP23A, 12 more genes
    nsv3128629copy number variation2nstd151human GRCh37 (hg19) chr1: 1,444,584-1,509,942 , GRCh38 (hg38) chr1: 1,509,204-1,574,562 SSU72, ATAD3A, 2 more genes
    nsv3120186copy number variation1nstd151human GRCh37 (hg19) chr7: 117,375,320-124,503,699 , GRCh38 (hg38) chr7: 117,735,266-124,863,645 NDUFA5, PTPRZ1, 71 more genes
    nsv3110041copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr1: 849,466-8,901,938 , GRCh38 (hg38) chr1: 914,086-8,841,879 , NCBI36 (hg18) chr1: 839,329-8,824,525 SSU72, LOC107984872, 215 more genes
    nsv3110040copy number variation1nstd37humanPathogenic NCBI36 (hg18) chr1: 836,543-3,987,287 , GRCh37 (hg19) chr1: 846,680-4,087,427 , GRCh38 (hg38) chr1: 911,300-4,027,367 SSU72, LOC105378591, 142 more genes
    nsv3110006copy number variation1nstd37humanUncertain significance NCBI36 (hg18) chr11: 3,949,918-4,989,260 , GRCh37 (hg19) chr11: 3,993,342-5,032,684 , GRCh38 (hg38) chr11: 3,972,112-5,011,454 STIM1, OR52Y1P, 57 more genes
    nsv3109988copy number variation1nstd37humanPathogenic NCBI36 (hg18) chrX: 72,986,649-154,881,025 , GRCh37 (hg19) chrX: 73,069,924-155,227,831 , GRCh38 (hg38) chrX: 73,850,089-155,998,166 RNU6-496P, RPL7L1P11, 1165 more genes
    nsv3109924copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr1: 849,466-2,330,338 , GRCh38 (hg38) chr1: 914,086-2,398,899 , NCBI36 (hg18) chr1: 839,329-2,320,198 SSU72, AGRN, 90 more genes
    nsv3109923copy number variation1nstd37humanPathogenic NCBI36 (hg18) chr1: 836,543-3,394,283 , GRCh37 (hg19) chr1: 846,680-3,404,423 , GRCh38 (hg38) chr1: 911,300-3,487,859 SSU72, C1QTNF12, 121 more genes
    nsv3109772copy number variation1nstd37humanPathogenic GRCh37 (hg19) chrX: 112,474,054-155,233,731 , GRCh38 (hg38) chrX: 113,230,827-156,004,066 , NCBI36 (hg18) chrX: 112,360,710-154,886,925 CSAG4, HSFX4, 717 more genes
    nsv3073852mobile element insertion1nstd144human GRCh37 (hg19) chr11: 4,253,298-4,253,298 , GRCh38 (hg38) chr11: 4,232,068-4,232,068 SSU72P5
    nsv3073564mobile element insertion1nstd144human GRCh37 (hg19) chr11: 4,262,391-4,262,391 , GRCh38 (hg38) chr11: 4,241,161-4,241,161 SSU72P2
    nsv3069775insertion1nstd90human GRCh37 (hg19) chr1: 1,479,107-1,479,108 , GRCh38 (hg38) chr1: 1,543,727-1,543,728 SSU72
    nsv3065702insertion1nstd140human GRCh37 (hg19) chr1: 1,501,011-1,501,012 , GRCh38 (hg38) chr1: 1,565,631-1,565,632 SSU72
    nsv3051619insertion1nstd140human GRCh38 (hg38) chr1: 1,565,682-1,565,683 , GRCh37 (hg19) chr1: 1,501,062-1,501,063 SSU72
    nsv2800880insertion1nstd137human GRCh38 (hg38) chr1: 1,543,726-1,543,726 , GRCh37 (hg19) chr1: 1,479,106-1,479,106 SSU72
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