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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3884782copy number variation1nstd102humanPathogenic GRCh37 chr10: 13,151,103-13,178,886 , GRCh38 chr10: 13,109,103-13,136,886 OPTN
    nsv6308984copy number variation1nstd102humanPathogenic GRCh37 chr10: 13,151,123-13,178,866 , GRCh38.p12 chr10: 13,109,123-13,136,866 OPTN
    nsv6309060copy number variation1nstd102humanPathogenic GRCh37 chr10: 13,152,254-13,161,060 , GRCh38.p12 chr10: 13,110,254-13,119,060 OPTN
    nsv7093782copy number variation1nstd102humanPathogenic GRCh37 chr10: 13,151,123-13,158,360 , GRCh38.p12 chr10: 13,109,123-13,116,360 OPTN
    nsv7093706copy number variation1nstd102humanPathogenic GRCh37 chr10: 13,154,433-13,161,060 , GRCh38.p12 chr10: 13,112,433-13,119,060 OPTN
    nsv7093783copy number variation1nstd102humanPathogenic GRCh37 chr10: 13,164,365-13,168,059 , GRCh38.p12 chr10: 13,122,365-13,126,059 OPTN
    nsv4681301copy number variation1nstd102humanPathogenic GRCh37 chr10: 13,151,113-13,154,645 , GRCh38.p12 chr10: 13,109,113-13,112,645 OPTN
    nsv6308985copy number variation1nstd102humanPathogenic GRCh37 chr10: 13,158,247-13,158,360 , GRCh38.p12 chr10: 13,116,247-13,116,360 OPTN
    nsv4681032copy number variation1nstd102humanPathogenic GRCh37 chr10: 13,158,257-13,158,350 , GRCh38.p12 chr10: 13,116,257-13,116,350 OPTN
    nsv7093866copy number variation1nstd102humanLikely pathogenic GRCh37 chr10: 13,152,353-13,162,081 , GRCh38.p12 chr10: 13,110,353-13,120,081 OPTN
    nsv6309140copy number variation2nstd102humanUncertain significance GRCh37 chr10: 13,160,868-13,161,060 , GRCh38.p12 chr10: 13,118,868-13,119,060 OPTN
    nsv4681859copy number variation1nstd102humanUncertain significance GRCh37 chr10: 13,160,878-13,161,050 , GRCh38.p12 chr10: 13,118,878-13,119,050 OPTN
    nsv7093625copy number variation1nstd102humanUncertain significance GRCh37 chr10: 13,158,247-13,169,923 , GRCh38.p12 chr10: 13,116,247-13,127,923 OPTN
    nsv6308901copy number variation1nstd102humanUncertain significance GRCh37 chr10: 13,151,123-13,154,655 , GRCh38.p12 chr10: 13,109,123-13,112,655 OPTN
    nsv3871156copy number variation1nstd102humanBenign GRCh37 chr2: 38,280,021-38,303,019 , GRCh38.p12 chr2: 38,052,878-38,075,877 CYP1B1, RMDN2
    nsv3877699copy number variation1nstd102humanPathogenic GRCh37 chr10: 13,151,123-13,225,100 , GRCh38 chr10: 13,109,123-13,183,100 OPTN, MCM10, 2 more genes
    nsv3886628copy number variation1nstd102humanUncertain significance GRCh37 chr2: 38,092,623-38,340,684 , GRCh38.p12 chr2: 37,865,480-38,113,542 CYP1B1, RMDN2, 3 more genes
    nsv3884418copy number variation1nstd102humanUncertain significance GRCh37 chr2: 38,232,794-38,359,795 , GRCh38.p12 chr2: 38,005,651-38,132,653 CYP1B1, RMDN2, 3 more genes
    nsv3889073copy number variation1nstd102humanUncertain significance GRCh37 chr2: 38,206,638-38,332,303 , GRCh38.p12 chr2: 37,979,495-38,105,161 CYP1B1, RMDN2-AS1, 2 more genes
    nsv4454718copy number variation1nstd102humanUncertain significance GRCh37 chr2: 38,291,099-38,373,417 , GRCh38.p12 chr2: 38,063,956-38,146,275 CYP1B1, RMDN2, 3 more genes
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