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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148054copy number variation1nstd102humanPathogenic GRCh37 chr1: 142,535,935-157,648,813 , GRCh38.p12 chr1: 120,175,847-149,601,750 , TRN-GTT12-1, 266 more genes
    nsv7137086copy number variation1nstd102humanPathogenic GRCh37 chr1: 146,465,878-147,416,212 , GRCh38.p12 chr1: 146,994,332-147,944,098 SSBL4P, OR13Z2P, 28 more genes
    nsv7098839copy number variation1nstd102humanPathogenic GRCh37 chr1: 146,405,854-147,597,284 , GRCh38.p12 chr1: 145,598,009-149,077,123 CCT8P1, LINC01719, 120 more genes
    nsv7098724copy number variation1nstd102humanPathogenic GRCh37 chr1: 146,397,357-148,344,744 , GRCh38.p12 chr1: 144,536,526-148,549,211 , LOC105371217, 150 more genes
    nsv7056440inversion1nstd229human GRCh37.p13 chr1|NW_003871055.3: 3,805,788-3,914,927 , GRCh38 chr1: 146,990,375-147,099,514 , GRCh37.p13 chr1: 146,464,012-146,571,098 NBPF13P, LOC644060, 7 more genes
    nsv7056211inversion1nstd229human GRCh38 chr1: 143,881,700-152,159,818 , GRCh37.p13 chr1|NW_003871055.3: 697,113-7,283,150 , PDIA3P1, 333 more genes
    nsv7045394inversion1nstd229human GRCh38 chr1: 143,732,174-147,339,264 , GRCh37.p13 chr1|NW_003871055.3: 547,587-4,154,677 , MIR6736, 130 more genes
    nsv6641804copy number variation1nstd229human GRCh38 chr1: 146,963,574-146,969,840 , GRCh37.p13 chr1: 146,247,626-146,253,299 , GRCh37.p13 chr1|NW_003871055.3: 3,778,987-3,785,253 NBPF12
    nsv6641803copy number variation1nstd229human GRCh38 chr1: 146,962,801-146,970,300 , GRCh37.p13 chr1|NW_003871055.3: 3,778,214-3,785,713 , GRCh37.p13 chr1: 146,247,166-146,253,299 NBPF12
    nsv6641802copy number variation1nstd229human GRCh38 chr1: 146,962,101-146,970,200 , GRCh37.p13 chr1: 146,247,266-146,253,299 , GRCh37.p13 chr1|NW_003871055.3: 3,777,514-3,785,613 NBPF12
    nsv6641637copy number variation1nstd229human GRCh38 chr1: 146,962,701-146,970,300 , GRCh37.p13 chr1|NW_003871055.3: 3,778,114-3,785,713 , GRCh37.p13 chr1: 146,247,166-146,253,299 NBPF12
    nsv6641468copy number variation1nstd229human GRCh38 chr1: 146,962,301-146,970,200 , GRCh37.p13 chr1|NW_003871055.3: 3,777,714-3,785,613 , GRCh37.p13 chr1: 146,247,266-146,253,299 NBPF12
    nsv6641376copy number variation1nstd229human GRCh38 chr1: 146,963,701-146,970,500 , GRCh37.p13 chr1: 146,246,966-146,253,299 , GRCh37.p13 chr1|NW_003871055.3: 3,779,114-3,785,913 NBPF12
    nsv6636744copy number variation1nstd102humanPathogenic GRCh37 chr1: 146,493,131-147,831,043 , GRCh38.p12 chr1: 145,430,980-148,358,916 PDZK1, ANKRD34A, 102 more genes
    nsv6634386copy number variation1nstd102humanPathogenic GRCh37 chr1: 146,626,685-147,597,284 , GRCh38.p12 chr1: 145,430,980-148,125,001 LOC391092, NBPF10, 84 more genes
    nsv6634349copy number variation1nstd102humanPathogenic GRCh37 chr1: 145,157,447-148,016,122 , GRCh38.p12 chr1: 144,536,526-149,492,442 , TRN-GTT10-1, 170 more genes
    nsv6545815inversion1nstd223human GRCh38 chr1: 146,946,539-148,140,447 , GRCh37.p13 chr1|NW_003871055.3: 3,761,952-4,955,860 , LOC391092, 39 more genes
    nsv6335368copy number variation1nstd223human GRCh38 chr1: 146,970,001-146,976,600 , GRCh37.p13 chr1|NW_003871055.3: 3,785,414-3,792,013 NBPF12
    nsv6335367copy number variation1nstd223human GRCh38 chr1: 146,961,637-146,967,924 , GRCh37.p13 chr1: 146,249,542-146,253,299 , GRCh37.p13 chr1|NW_003871055.3: 3,777,050-3,783,337 NBPF12
    nsv6335276copy number variation1nstd223human GRCh38 chr1: 146,968,101-146,969,900 , GRCh37.p13 chr1: 146,247,566-146,249,365 , GRCh37.p13 chr1|NW_003871055.3: 3,783,514-3,785,313 NBPF12
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