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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
    nsv7148051copy number variation1nstd102humanPathogenic GRCh37 chr1: 146,474,687-147,415,708 , GRCh38.p12 chr1: 147,003,128-147,943,594 LOC728989, RNU1-151P, 27 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
    nsv7099229copy number variation1nstd231human GRCh38.p12 chr1: 147,122,321-147,688,905 , GRCh37 chr1: 146,593,903-147,161,023 BCL9, FMO5, 12 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
    nsv7056211inversion1nstd229human GRCh38 chr1: 143,881,700-152,159,818 , GRCh37.p13 chr1|NW_003871055.3: 697,113-7,283,150 , PDIA3P1, 333 more genes
    nsv7044037inversion1nstd229human GRCh38 chr1: 147,326,086-147,597,011 , GRCh37.p13 chr1: 146,797,813-147,068,804 , GRCh37.p13 chr1|NW_003871055.3: 4,141,499-4,412,424 OR13Z2P, BCL9, 3 more genes
    nsv6641871copy number variation1nstd229human GRCh38 chr1: 147,577,501-147,780,600 , GRCh37.p13 chr1|NW_003871055.3: 4,392,914-4,596,013 , GRCh37.p13 chr1: 147,049,293-147,252,711 GJA5, BCL9, 4 more genes
    nsv6641870copy number variation1nstd229human GRCh38 chr1: 147,534,855-147,540,646 , GRCh37.p13 chr1|NW_003871055.3: 4,350,268-4,356,059 , GRCh37.p13 chr1: 147,006,673-147,012,473 BCL9
    nsv6641827copy number variation1nstd229human GRCh38 chr1: 147,568,866-147,569,012 , GRCh37.p13 chr1|NW_003871055.3: 4,384,279-4,384,425 , GRCh37.p13 chr1: 147,040,648-147,040,794 BCL9
    nsv6641491copy number variation1nstd229human GRCh38 chr1: 147,616,657-147,618,504 , GRCh37.p13 chr1|NW_003871055.3: 4,432,070-4,433,917 , GRCh37.p13 chr1: 147,088,457-147,090,309 BCL9
    nsv6641490copy number variation1nstd229human GRCh38 chr1: 147,608,332-147,610,737 , GRCh37.p13 chr1|NW_003871055.3: 4,423,745-4,426,150 , GRCh37.p13 chr1: 147,080,129-147,082,536 BCL9
    nsv6636869copy number variation1nstd102humanPathogenic GRCh37 chr1: 146,498,299-147,393,336 , GRCh38.p12 chr1: 147,026,742-147,921,222 LOC391092, PRKAB2, 26 more genes
    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
    nsv6547513inversion1nstd223human GRCh38 chr1: 147,583,452-147,583,838 , GRCh37.p13 chr1: 147,055,252-147,055,638 , GRCh37.p13 chr1|NW_003871055.3: 4,398,865-4,399,251 BCL9
    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
    nsv6542731inversion1nstd223human GRCh38 chr1: 147,056,374-148,969,054 , GRCh37.p13 chr1|NW_003871055.3: 3,871,787-5,784,467 , LINC01731, 75 more genes
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