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Items: 1 to 20 of 369

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6129329insertion1nstd186human GRCh37 chr17: 17,155,784-17,155,808 , GRCh38.p12 chr17: 17,252,470-17,252,494 COPS3
    nsv5974534inversion1nstd209human GRCh38 chr17: 15,750,079-18,634,890 , GRCh37.p13 chr17: 15,653,393-18,538,203 , ADORA2B, 119 more genes
    nsv5974143insertion1nstd209human GRCh38 chr17: 17,258,591-17,258,591 , GRCh37.p13 chr17: 17,161,905-17,161,905 COPS3
    nsv5939146copy number variation1nstd209human GRCh38 chr17: 17,252,332-17,252,436 , GRCh37.p13 chr17: 17,155,646-17,155,750 COPS3
    nsv5933579copy number variation1nstd209human GRCh38 chr17: 16,936,959-20,558,118 , GRCh37.p13 chr17: 16,840,273-20,461,431 , FAM106B, 146 more genes
    nsv5929290copy number variation1nstd209human GRCh38 chr17: 17,277,505-17,277,641 , GRCh37.p13 chr17: 17,180,819-17,180,955 COPS3
    nsv5700482mobile element insertion2nstd211human GRCh38 chr17: 17,279,611-17,279,611 , GRCh37.p13 chr17: 17,182,925-17,182,925 COPS3
    nsv5665112inversion1nstd207human GRCh37.p13 chr17: 16,704,599-18,417,421 , GRCh38 chr17: 16,801,285-18,514,107 , DRG2, 71 more genes
    nsv5650337insertion1nstd207human GRCh38 chr17: 17,279,597-17,279,597 , GRCh37.p13 chr17: 17,182,911-17,182,911 COPS3
    nsv5645366insertion1nstd207human GRCh38 chr17: 17,252,362-17,252,362 , GRCh37.p13 chr17: 17,155,676-17,155,676 COPS3
    nsv5602488copy number variation1nstd207human GRCh38 chr17: 17,252,332-17,252,401 , GRCh37.p13 chr17: 17,155,646-17,155,715 COPS3
    nsv5557263sequence alteration1nstd206human GRCh38 chr17: 17,251,812-17,332,027 , GRCh37.p13 chr17: 17,155,126-17,235,341 COPS3, NT5M
    nsv5544967insertion1nstd206human GRCh38 chr17: 17,252,470-17,252,494 , GRCh37.p13 chr17: 17,155,784-17,155,808 COPS3
    nsv5532635copy number variation1nstd206human GRCh38 chr17: 17,259,963-17,260,048 , GRCh37.p13 chr17: 17,163,277-17,163,362 COPS3
    nsv5520233copy number variation1nstd206human GRCh38 chr17: 17,261,907-17,282,405 , GRCh37.p13 chr17: 17,165,221-17,185,719 COPS3
    nsv5415230mobile element insertion1nstd206human GRCh38 chr17: 17,279,611-17,279,662 , GRCh37.p13 chr17: 17,182,925-17,182,976 COPS3
    nsv5381800copy number variation1nstd102humanPathogenic GRCh37 chr17: 16,601,603-20,063,369 , GRCh38.p12 chr17: 16,698,289-20,160,056 COTL1P1, LOC105371551, 141 more genes
    nsv5381797copy number variation1nstd102humanPathogenic GRCh37 chr17: 17,145,361-20,137,943 , GRCh38.p12 chr17: 17,242,047-20,234,630 LOC644909, FLII, 117 more genes
    nsv5381795copy number variation1nstd102humanUncertain significance GRCh37 chr17: 17,104,302-17,690,077 , GRCh38.p12 chr17: 17,200,988-17,786,763 RPL13P12, ACTG1P24, 15 more genes
    nsv5149876mobile element insertion1nstd203human GRCh38 chr17: 17,258,591-17,258,607 , GRCh37.p13 chr17: 17,161,905-17,161,921 COPS3
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