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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
    nsv7045394inversion1nstd229human GRCh38 chr1: 143,732,174-147,339,264 , GRCh37.p13 chr1|NW_003871055.3: 547,587-4,154,677 , MIR6736, 130 more genes
    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
    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
    nsv6333880copy number variation1nstd223human GRCh38 chr1: 145,488,103-148,061,210 , GRCh37.p13 chr1|NW_003871055.3: 2,303,516-4,876,623 , TRR-CCT6-2, 79 more genes
    nsv6324605copy number variation1nstd223human GRCh38 chr1: 147,168,101-147,182,100 , GRCh37.p13 chr1|NW_003871055.3: 3,983,514-3,997,513 , GRCh37.p13 chr1: 146,639,680-146,653,680 FMO5, PRKAB2, 2 more genes
    nsv6314909copy number variation1nstd102humanPathogenic GRCh38 chr1: 147,050,137-148,438,699 , GRCh37.p13 chr1|NW_003871055.3: 3,865,550-5,254,112 LOC101927468, MIR5087, 61 more genes
    nsv6290404copy number variation1nstd102humanPathogenic GRCh37 chr1: 146,043,714-148,514,899 , GRCh38.p12 chr1: 144,536,526-148,549,211 , TRN-GTT9-2, 150 more genes
    nsv6290073copy number variation1nstd218human GRCh38.p12 chr1: 143,511,409-149,082,254 , GRCh37 chr1: 147,824,148-149,378,266 , BCL9, 215 more genes
    nsv6290072copy number variation1nstd218human GRCh38.p12 chr16: 34,632,766-36,225,009 , GRCh38.p12 chr7: 61,006,478-62,429,617 , GRCh38.p12 chr1: 146,347,888-148,514,931 , GRCh37 chr1: 147,806,599-149,821,717 , BCL9, 149 more genes
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