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Items: 1 to 20 of 298

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7073320inversion1nstd229human GRCh38 chr21: 13,847,649-13,848,557 , GRCh37.p13 chr21: 15,219,970-15,220,878 CYP4F29P
    nsv7066087inversion1nstd229human GRCh38 chr21: 13,504,952-14,129,881 , GRCh37.p13 chr21: 14,877,273-15,502,202 CYP4F29P, ANKRD20A18P, 32 more genes
    nsv7036629copy number variation1nstd229human GRCh38 chr21: 13,343,077-14,140,383 , GRCh37.p13 chr21: 14,715,398-15,512,704 ANKRD20A18P, ERLEC1P1, 37 more genes
    nsv7032372copy number variation1nstd229human GRCh38 chr21: 13,843,889-13,843,934 , GRCh37.p13 chr21: 15,216,210-15,216,255 CYP4F29P
    nsv6637761copy number variation1nstd102humanUncertain significance GRCh37 chr21: 15,006,458-21,778,529 , GRCh38.p12 chr21: 13,634,137-20,406,217 ASMER1, ERLEC1P1, 91 more genes
    nsv6637251copy number variation1nstd102humanUncertain significance GRCh37 chr21: 15,023,402-17,685,941 , GRCh38.p12 chr21: 13,651,081-16,313,620 LOC105369292, ABCC13, 51 more genes
    nsv6634469copy number variation1nstd102humanPathogenic GRCh37 chr21: 15,006,457-29,046,428 , GRCh38.p12 chr21: 13,634,136-27,674,109 ADAMTS5, VN2R20P, 160 more genes
    nsv6626848copy number variation1nstd224human GRCh37 chr21: 15,214,708-15,275,981 , GRCh38.p12 chr21: 13,842,387-13,903,660 CYP4F29P
    nsv6626847copy number variation4nstd224human GRCh37 chr21: 14,669,931-15,275,981 , GRCh38.p12 chr21: 13,297,610-13,903,660 CYP4F29P, TERF1P1, 24 more genes
    nsv6626816copy number variation1nstd224human GRCh37 chr21: 14,610,372-15,216,110 , GRCh38.p12 chr21: 13,238,051-13,843,789 VN1R8P, OR4K11P, 24 more genes
    nsv6626739copy number variation1nstd224human GRCh37 chr21: 14,670,124-15,255,792 , GRCh38.p12 chr21: 13,297,803-13,883,471 CYP4F29P, OR4K11P, 24 more genes
    nsv6626738copy number variation1nstd224human GRCh37 chr21: 14,670,124-15,216,110 , GRCh38.p12 chr21: 13,297,803-13,843,789 VN1R8P, GXYLT1P2, 24 more genes
    nsv6626737copy number variation2nstd224human GRCh37 chr21: 14,669,931-15,216,154 , GRCh38.p12 chr21: 13,297,610-13,843,833 OR4K11P, GTF2IP2, 24 more genes
    nsv6626736copy number variation3nstd224human GRCh37 chr21: 14,595,742-15,263,760 , GRCh38.p12 chr21: 13,223,421-13,891,439 CYP4F29P, POTED, 24 more genes
    nsv6626624copy number variation1nstd224human GRCh37 chr21: 1-48,129,895 , GRCh38.p12 chr21: 8,522,361-46,699,983 , ATP5PO, 657 more genes
    nsv6626620copy number variation1nstd224human GRCh37 chr21: 15,153,902-15,235,277 , GRCh38.p12 chr21: 13,781,581-13,862,956 CYP4F29P, CNN2P7, 4 more genes
    nsv6626619copy number variation1nstd224human GRCh37 chr21: 15,153,902-15,224,474 , GRCh38.p12 chr21: 13,781,581-13,852,153 CYP4F29P, CNN2P7, 4 more genes
    nsv6626618copy number variation2nstd224human GRCh37 chr21: 14,669,931-15,216,275 , GRCh38.p12 chr21: 13,297,610-13,843,954 CYP4F29P, POTED, 24 more genes
    nsv6626617copy number variation1nstd224human GRCh37 chr21: 14,669,931-15,215,814 , GRCh38.p12 chr21: 13,297,610-13,843,493 POTED, CNN2P7, 24 more genes
    nsv6626616copy number variation1nstd224human GRCh37 chr21: 14,595,742-15,258,717 , GRCh38.p12 chr21: 13,223,421-13,886,396 OR4K12P, SNX19P1, 24 more genes
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