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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
    nsv7050259inversion1nstd229human GRCh38 chr1: 147,193,519-147,200,055 , GRCh37.p13 chr1|NW_003871055.3: 4,008,932-4,015,468 , GRCh37.p13 chr1: 146,665,098-146,671,636 FMO5, CHD1L
    nsv7045394inversion1nstd229human GRCh38 chr1: 143,732,174-147,339,264 , GRCh37.p13 chr1|NW_003871055.3: 547,587-4,154,677 , MIR6736, 130 more genes
    nsv6641814copy number variation1nstd229human GRCh38 chr1: 147,189,087-147,198,575 , GRCh37.p13 chr1|NW_003871055.3: 4,004,500-4,013,988 , GRCh37.p13 chr1: 146,660,667-146,670,154 FMO5, CHD1L
    nsv6641639copy number variation1nstd229human GRCh38 chr1: 147,188,301-147,198,700 , GRCh37.p13 chr1|NW_003871055.3: 4,003,714-4,014,113 , GRCh37.p13 chr1: 146,659,880-146,670,279 CHD1L, FMO5
    nsv6641475copy number variation1nstd229human GRCh38 chr1: 147,210,483-147,213,406 , GRCh37.p13 chr1|NW_003871055.3: 4,025,896-4,028,819 , GRCh37.p13 chr1: 146,682,051-146,684,973 CHD1L, FMO5
    nsv6641474copy number variation1nstd229human GRCh38 chr1: 147,189,201-147,198,600 , GRCh37.p13 chr1: 146,660,781-146,670,179 , GRCh37.p13 chr1|NW_003871055.3: 4,004,614-4,014,013 CHD1L, FMO5
    nsv6641385copy number variation1nstd229human GRCh38 chr1: 147,215,795-147,220,519 , GRCh37.p13 chr1|NW_003871055.3: 4,031,208-4,035,932 , GRCh37.p13 chr1: 146,687,365-146,692,097 CHD1L, FMO5
    nsv6641384copy number variation1nstd229human GRCh38 chr1: 147,210,900-147,215,522 , GRCh37.p13 chr1|NW_003871055.3: 4,026,313-4,030,935 , GRCh37.p13 chr1: 146,682,468-146,687,092 CHD1L, FMO5
    nsv6641383copy number variation1nstd229human GRCh38 chr1: 147,193,601-147,197,600 , GRCh37.p13 chr1|NW_003871055.3: 4,009,014-4,013,013 , GRCh37.p13 chr1: 146,665,180-146,669,179 CHD1L, FMO5
    nsv6641382copy number variation1nstd229human GRCh38 chr1: 147,187,801-147,198,700 , GRCh37.p13 chr1: 146,659,380-146,670,279 , GRCh37.p13 chr1|NW_003871055.3: 4,003,214-4,014,113 FMO5, CHD1L
    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
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