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Items: 1 to 20 of 738

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148083copy number variation1nstd102humanUncertain significance GRCh37 chr1: 145,646,115-145,826,929 , GRCh38.p12 chr1: 145,608,134-145,788,966 RNF115, PDZK1, 3 more genes
    nsv7148064copy number variation1nstd102humanPathogenic GRCh37 chr1: 145,365,275-145,826,979 , GRCh38.p12 chr1: 145,608,084-146,069,727 ANKRD34A, RNVU1-6, 26 more genes
    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
    nsv7137200copy number variation1nstd102humanPathogenic GRCh37 chr1: 145,382,123-145,792,051 , GRCh38.p12 chr1: 145,642,989-146,052,881 PDZK1, LOC107985593, 24 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
    nsv7098747copy number variation1nstd102humanPathogenic GRCh37 chr1: 145,414,780-145,826,931 , GRCh38.p12 chr1: 145,608,132-146,020,233 TXNIP, CD160, 19 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
    nsv7057592inversion1nstd229human GRCh38 chr1: 145,720,190-145,720,306 , GRCh37.p13 chr1: 145,714,779-145,714,895 , GRCh37.p13 chr1|NW_003871055.3: 2,535,603-2,535,719 CD160
    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
    nsv7045117inversion1nstd229human GRCh38 chr1: 143,671,956-145,963,983 , GRCh37.p13 chr1|NW_003871055.3: 487,369-2,779,396 , GPR89A, 96 more genes
    nsv6641560copy number variation1nstd229human GRCh38 chr1: 145,425,707-145,882,259 , GRCh37.p13 chr1|NW_003871055.3: 2,241,120-2,697,672 , GRCh37.p13 chr1: 145,552,817-145,833,118 , CD160, 15 more genes
    nsv6637126copy number variation1nstd102humanUncertain significance GRCh37 chr1: 145,617,349-145,888,926 , GRCh38.p12 chr1: 145,601,946-145,817,743 RNF115, GPR89A, 3 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
    nsv6636705copy number variation1nstd102humanUncertain significance GRCh37 chr1: 145,621,908-145,808,309 , GRCh38.p12 chr1: 145,626,745-145,813,185 GPR89A, RNF115, 2 more genes
    nsv6636507copy number variation1nstd102humanUncertain significance GRCh37 chr1: 145,608,099-145,888,926 , GRCh38.p12 chr1: 145,601,946-145,827,014 GPR89A, NBPF25P, 4 more genes
    nsv6636370copy number variation1nstd102humanUncertain significance GRCh37 chr1: 145,622,531-145,888,926 , GRCh38.p12 chr1: 145,601,946-145,812,561 GPR89A, PDZK1, 3 more genes
    nsv6635359copy number variation2nstd227human GRCh38.p12 chr1: 145,672,100-145,809,105 , GRCh37 chr1: 145,625,979-145,762,959 PDZK1, CD160, 1 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
    nsv6634368copy number variation1nstd102humanPathogenic GRCh37 chr1: 145,387,023-145,764,679 , GRCh38.p12 chr1: 145,670,380-146,047,980 TRK-CTT2-1, TXNIP, 22 more genes
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