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Items: 1 to 20 of 523

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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
    nsv6641873copy number variation1nstd229human GRCh38 chr1: 147,627,664-147,628,468 , GRCh37.p13 chr1: 147,099,465-147,100,269 , GRCh37.p13 chr1|NW_003871055.3: 4,443,077-4,443,881 ACP6
    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
    nsv6641829copy number variation1nstd229human GRCh38 chr1: 147,657,251-147,659,832 , GRCh37.p13 chr1|NW_003871055.3: 4,472,664-4,475,245 , GRCh37.p13 chr1: 147,129,366-147,131,947 ACP6
    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
    nsv6545061inversion1nstd223human GRCh38 chr1: 147,667,420-147,667,984 , GRCh37.p13 chr1: 147,139,539-147,140,103 , GRCh37.p13 chr1|NW_003871055.3: 4,482,833-4,483,397 ACP6
    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
    nsv6333013copy number variation1nstd223human GRCh38 chr1: 147,658,531-147,659,273 , GRCh37.p13 chr1: 147,130,646-147,131,388 , GRCh37.p13 chr1|NW_003871055.3: 4,473,944-4,474,686 ACP6
    nsv6332958copy number variation1nstd223human GRCh38 chr1: 147,652,889-147,653,193 , GRCh37.p13 chr1|NW_003871055.3: 4,468,302-4,468,606 ACP6
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