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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3957887copy number variation1nstd168human GRCh38 (hg38) chr10: 119,354,744-119,369,523 , GRCh37.p13 chr10: 121,114,256-121,129,035 GRK5
    nsv3951292insertion1nstd167human GRCh37 (hg19) chr10: 121,020,582-121,020,582 , GRCh38.p12 chr10: 119,261,070-119,261,070 GRK5
    nsv3943725insertion1nstd167human GRCh37 (hg19) chr10: 121,072,559-121,072,559 , GRCh38.p12 chr10: 119,313,047-119,313,047 GRK5
    nsv3941863insertion1nstd167human GRCh37 (hg19) chr10: 121,072,451-121,072,451 , GRCh38.p12 chr10: 119,312,939-119,312,939 GRK5
    nsv3932785copy number variation1nstd167human GRCh37 (hg19) chr10: 121,046,835-121,046,886 , GRCh38.p12 chr10: 119,287,323-119,287,374 GRK5
    nsv3931471copy number variation1nstd167human GRCh37 (hg19) chr10: 121,154,053-121,154,107 , GRCh38.p12 chr10: 119,394,541-119,394,595 GRK5
    nsv3929876insertion1nstd167human GRCh37 (hg19) chr10: 121,186,822-121,186,822 , GRCh38.p12 chr10: 119,427,310-119,427,310 GRK5
    nsv3923859copy number variation1nstd102humanPathogenic GRCh38 (hg38) chr10: 111,313,099-133,620,674 , GRCh37.p13 chr10: 113,072,857-135,434,178 , NCBI36 (hg18) chr10: 113,062,847-135,284,168 GRK5, ALDOAP2, 348 more genes
    nsv3923769copy number variation1nstd102humanPathogenic GRCh38 (hg38) chr10: 100,194,215-132,432,797 , GRCh37.p13 chr10: 101,953,972-134,246,301 , NCBI36 (hg18) chr10: 101,943,962-134,096,291 GRK5, ACADSB, 496 more genes
    nsv3922274copy number variation1nstd102humanUncertain significance NCBI36 (hg18) chr10: 103,274,160-135,374,737 , GRCh37.p13 chr10: 103,284,170-135,524,747 , GRCh38.p12 chr10: 101,524,413-133,787,422 GRK5, ADAM8, 526 more genes
    nsv3921919copy number variation1nstd102humanPathogenic GRCh38 (hg38) chr10: 100,600,492-133,622,588 , GRCh37.p13 chr10: 102,360,249-135,436,092 , NCBI36 (hg18) chr10: 102,350,239-135,286,082 GRK5, ACADSB, 529 more genes
    nsv3920295copy number variation1nstd102humanPathogenic NCBI36 (hg18) chr10: 81,675,342-135,374,737 , GRCh37.p13 chr10: 81,685,362-135,524,747 , GRCh38.p12 chr10: 79,925,606-133,787,422 GRK5, ACTA2, 923 more genes
    nsv3919647copy number variation1nstd102humanPathogenic GRCh38 (hg38) chr10: 106,925,303-133,620,815 , GRCh37.p13 chr10: 108,685,061-135,434,319 , NCBI36 (hg18) chr10: 108,675,051-135,284,309 GRK5, ACADSB, 397 more genes
    nsv3919460copy number variation1nstd102humanUncertain significance GRCh38 (hg38) chr10: 118,832,386-119,400,019 , GRCh37.p13 chr10: 120,591,898-121,159,531 , NCBI36 (hg18) chr10: 120,581,888-121,149,521 GRK5, RN7SL749P, 11 more genes
    nsv3919433copy number variation1nstd102humanUncertain significance NCBI36 (hg18) chr10: 119,668,832-121,236,830 , GRCh37.p13 chr10: 119,678,842-121,246,840 , GRCh38.p12 chr10: 117,919,331-119,487,328 GRK5, PRLHR, 24 more genes
    nsv3916721copy number variation1nstd102humanPathogenic GRCh38 (hg38) chr10: 119,273,012-123,117,390 , GRCh37.p13 chr10: 121,032,524-124,876,906 , NCBI36 (hg18) chr10: 121,022,514-124,866,896 GRK5, TACC2, 59 more genes
    nsv3914619copy number variation1nstd102humanPathogenic NCBI36 (hg18) chr10: 111,418,518-126,431,209 , GRCh37.p13 chr10: 111,428,528-126,441,219 , GRCh38.p12 chr10: 109,668,770-124,752,650 GRK5, ADRA2A, 235 more genes
    nsv3913997copy number variation1nstd102humanPathogenic GRCh38 (hg38) chr10: 117,866,565-133,554,210 , GRCh37.p13 chr10: 119,626,076-135,367,714 , NCBI36 (hg18) chr10: 119,616,066-135,217,704 GRK5, ALDOAP2, 251 more genes
    nsv3912079copy number variation1nstd102humanPathogenic GRCh38 (hg38) chr10: 108,102,587-133,620,674 , GRCh37.p13 chr10: 109,862,345-135,434,178 , NCBI36 (hg18) chr10: 109,852,335-135,284,168 GRK5, ADRA2A, 390 more genes
    nsv3911931copy number variation1nstd102humanPathogenic NCBI36 (hg18) chr10: 118,114,834-135,324,715 , GRCh37.p13 chr10: 118,124,844-135,474,725 , GRCh38.p12 chr10: 116,365,332-133,661,221 GRK5, CYP2E1, 286 more genes
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