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Items: 1 to 20 of 149

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3163107copy number variation1nstd151human GRCh37 (hg19) chr19: 3,204,568-3,207,691 , GRCh38 (hg38) chr19: 3,204,570-3,207,693 NCLN
    nsv3162806copy number variation1nstd151human GRCh37 (hg19) chr19: 3,205,934-3,207,491 , GRCh38 (hg38) chr19: 3,205,936-3,207,493 NCLN
    nsv3162419copy number variation1nstd151human GRCh37 (hg19) chr19: 3,203,751-3,207,691 , GRCh38 (hg38) chr19: 3,203,753-3,207,693 NCLN
    nsv3161712copy number variation1nstd151human GRCh37 (hg19) chr19: 3,205,934-3,207,691 , GRCh38 (hg38) chr19: 3,205,936-3,207,693 NCLN
    nsv2782658copy number variation1nstd132human NCBI36 (hg18) chr19: 3,142,604-3,167,946 , GRCh37 (hg19) chr19: 3,191,604-3,216,946 , GRCh38 (hg38) chr19: 3,191,606-3,216,948 NCLN
    nsv2779094copy number variation2nstd37humanPathogenic GRCh37 (hg19) chr19: 260,912-58,956,888 , GRCh38 (hg38) chr19: 260,912-58,445,521 , NCBI36 (hg18) chr19: 211,912-63,648,700 NCLN, TIMM29, 2463 more genes
    nsv2775280copy number variation1nstd37humanUncertain significance GRCh37 (hg19) chr19: 2,652,901-4,342,179 , GRCh38 (hg38) chr19: 2,652,903-4,342,182 , NCBI36 (hg18) chr19: 2,603,901-4,293,179 NCLN, GNA15, 65 more genes
    nsv2768219copy-neutral loss of heterozygosity1nstd125human GRCh38 (hg38) chr19: 260,911-20,692,745 , GRCh37 (hg19) chr19: 260,911-20,875,551 NCLN, ACP5, 918 more genes
    nsv2768218copy-neutral loss of heterozygosity1nstd125human GRCh38 (hg38) chr19: 260,911-19,745,645 , GRCh37 (hg19) chr19: 260,911-19,856,454 NCLN, ACP5, 870 more genes
    nsv2768217copy-neutral loss of heterozygosity1nstd125human GRCh38 (hg38) chr19: 260,911-16,062,156 , GRCh37 (hg19) chr19: 260,911-16,172,966 NCLN, ACP5, 727 more genes
    nsv2766848copy number variation1nstd130human NCBI36 (hg18) chr19: 341,627-8,021,720 , GRCh37 (hg19) chr19: 390,627-8,115,720 , GRCh38 (hg38) chr19: 390,627-8,050,836 NCLN, CD70, 336 more genes
    nsv2766828copy number variation1nstd130human GRCh37 (hg19) chr19: 3,189,278-3,208,890 , GRCh38 (hg38) chr19: 3,189,280-3,208,892 NCLN
    nsv2761311copy number variation1nstd130human NCBI36 (hg18) chr19: 341,627-5,078,398 , GRCh37 (hg19) chr19: 390,627-5,127,398 , GRCh38 (hg38) chr19: 390,627-5,127,387 NCLN, AES, 222 more genes
    nsv2760458copy number variation1nstd130human NCBI36 (hg18) chr19: 352,714-5,407,930 , GRCh37 (hg19) chr19: 401,714-5,456,930 , GRCh38 (hg38) chr19: 401,714-5,456,919 NCLN, AES, 227 more genes
    nsv2759751copy number variation1nstd130human NCBI36 (hg18) chr19: 323,661-5,662,930 , GRCh37 (hg19) chr19: 372,661-5,711,930 , GRCh38 (hg38) chr19: 372,661-5,711,919 NCLN, HCN2, 237 more genes
    nsv2758626copy number variation1nstd130human GRCh37 (hg19) chr19: 289,244-19,611,550 , GRCh38 (hg38) chr19: 289,244-19,500,741 NCLN, HCN2, 857 more genes
    nsv2758361copy number variation1nstd130human NCBI36 (hg18) chr19: 445,057-10,300,711 , GRCh37 (hg19) chr19: 494,057-10,439,711 , GRCh38 (hg38) chr19: 494,057-10,329,035 NCLN, AMH, 435 more genes
    nsv2757939copy number variation1nstd130human GRCh37 (hg19) chr19: 392,023-19,291,184 , GRCh38 (hg38) chr19: 392,023-19,180,375 NCLN, AZU1, 844 more genes
    nsv2757729copy number variation1nstd130human GRCh37 (hg19) chr19: 400,926-11,618,630 , GRCh38 (hg38) chr19: 400,926-11,507,815 NCLN, AES, 491 more genes
    nsv2757532copy number variation1nstd130human GRCh37 (hg19) chr19: 266,034-54,723,310 , GRCh38 (hg38) chr19: 266,034-54,160,365 NCLN, ACP5, 2221 more genes
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