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Items: 1 to 20 of 234

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3148437copy number variation1nstd151human GRCh37 (hg19) chr9: 37,708,393-38,016,133 , GRCh38 (hg38) chr9: 37,708,396-38,016,136 DCAF10, SHB, 9 more genes
    nsv3139508copy number variation1nstd151human GRCh37 (hg19) chr9: 37,724,219-38,016,133 , GRCh38 (hg38) chr9: 37,724,222-38,016,136 DCAF10, RNU7-124P, 9 more genes
    nsv3069503insertion1nstd90human GRCh37 (hg19) chr9: 37,808,747-37,808,748 , GRCh38 (hg38) chr9: 37,808,750-37,808,751 DCAF10
    nsv2818798insertion2nstd137human GRCh38 (hg38) chr9: 37,808,749-37,808,749 , GRCh37 (hg19) chr9: 37,808,746-37,808,746 DCAF10
    nsv2786231copy number variation1nstd132human NCBI36 (hg18) chr9: 37,821,556-37,859,282 , GRCh37 (hg19) chr9: 37,831,556-37,869,282 , GRCh38 (hg38) chr9: 37,831,559-37,869,285 DCAF10, MRPS10P5
    nsv2777670copy number variation1nstd37humanBenign NCBI36 (hg18) chr9: 47,102,101-70,161,607 , GRCh37 (hg19) chr9: 47,312,281-70,871,931 , GRCh38 (hg38) chr9: 193,412-68,356,871 DCAF10, ACO1, 883 more genes
    nsv2777269copy number variation2nstd37humanPathogenic GRCh37 (hg19) chr9: 203,861-38,787,480 , GRCh38 (hg38) chr9: 203,861-38,787,483 , NCBI36 (hg18) chr9: 193,861-38,777,480 DCAF10, RN7SL849P, 585 more genes
    nsv2776570copy number variation3nstd37humanBenign NCBI36 (hg18) chr9: 47,102,101-70,238,530 , GRCh37 (hg19) chr9: 47,312,281-70,871,931 , GRCh38 (hg38) chr9: 193,412-68,433,794 DCAF10, ANXA2P2, 884 more genes
    nsv2775336copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr9: 203,861-67,983,174 , GRCh38 (hg38) chr9: 203,861-68,257,015 , NCBI36 (hg18) chr9: 193,861-67,572,994 DCAF10, ANXA2P2, 881 more genes
    nsv2775104copy number variation1nstd37humanBenign NCBI36 (hg18) chr9: 47,102,101-70,250,706 , GRCh37 (hg19) chr9: 47,312,281-70,871,931 , GRCh38 (hg38) chr9: 193,412-68,445,970 DCAF10, PLIN2, 884 more genes
    nsv2774488copy number variation1nstd37humanPathogenic NCBI36 (hg18) chr9: 2,934-140,273,252 , GRCh37 (hg19) chr9: 12,934-141,153,431 , GRCh38 (hg38) chr9: 12,934-138,262,981 DCAF10, ABCA1, 2268 more genes
    nsv2773829copy number variation2nstd37humanBenign NCBI36 (hg18) chr9: 47,102,101-70,129,166 , GRCh37 (hg19) chr9: 47,312,281-70,871,931 , GRCh38 (hg38) chr9: 193,412-68,324,430 DCAF10, ACO1, 880 more genes
    nsv2773768copy number variation2nstd37humanPathogenic GRCh37 (hg19) chr9: 203,861-69,002,883 , GRCh38 (hg38) chr9: 203,861-68,257,015 , NCBI36 (hg18) chr9: 193,861-68,292,703 DCAF10, ALDH1B1, 881 more genes
    nsv2773513copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr9: 203,861-88,189,913 , GRCh38 (hg38) chr9: 203,861-85,574,998 , NCBI36 (hg18) chr9: 193,861-87,379,733 DCAF10, NFX1, 1101 more genes
    nsv2773152copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr9: 203,864-141,020,389 , GRCh38 (hg38) chr9: 203,864-138,125,937 , NCBI36 (hg18) chr9: 193,864-140,140,210 DCAF10, ABCA1, 2250 more genes
    nsv2772450copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr9: 203,861-68,188,391 , GRCh38 (hg38) chr9: 203,861-68,257,015 , NCBI36 (hg18) chr9: 193,861-67,678,211 DCAF10, ACO1, 881 more genes
    nsv2771898copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr9: 32,396-39,140,211 , GRCh38 (hg38) chr9: 32,396-39,140,214 , NCBI36 (hg18) chr9: 22,396-39,130,211 DCAF10, ACO1, 598 more genes
    nsv2771726copy number variation1nstd37humanPathogenic NCBI36 (hg18) chr9: 2,934-65,222,364 , GRCh37 (hg19) chr9: 12,934-65,482,544 , GRCh38 (hg38) chr9: 12,934-67,217,006 DCAF10, PLIN2, 877 more genes
    nsv2769134copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr9: 13,997-70,919,878 , GRCh38 (hg38) chr9: 13,997-68,304,962 , NCBI36 (hg18) chr9: 3,997-70,109,698 DCAF10, PLIN2, 896 more genes
    nsv2756841copy number variation1nstd130human GRCh37 (hg19) chr9: 502,292-140,777,105 , GRCh38 (hg38) chr9: 502,292-137,882,653 DCAF10, ABCA1, 2242 more genes
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