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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7073998inversion1nstd229human GRCh38 chr17: 32,918,710-41,148,753 , GRCh37.p13 chr17: 31,245,728-39,305,005 LOC105371750, C17orf78, 298 more genes
    nsv6995210copy number variation1nstd229human GRCh38 chr17: 38,770,587-39,362,529 , GRCh37.p13 chr17: 36,926,840-37,518,782 FBXL20, TRC-GCA2-3, 28 more genes
    nsv6984984copy number variation1nstd229human GRCh38 chr17: 38,377,708-42,855,253 , GRCh37.p13 chr17: 36,701,616-41,007,270 ZNF385C, AOC2, 248 more genes
    nsv6982861copy number variation1nstd229human GRCh38 chr17: 38,291,672-47,498,259 , GRCh37.p13 chr17: 36,510,266-45,575,625 KRT20, PLEKHH3, 442 more genes
    nsv6978978copy number variation1nstd229human GRCh38 chr17: 39,169,305-39,562,570 , GRCh37.p13 chr17: 37,325,558-37,718,823 STAC2, MIR548BC, 8 more genes
    nsv6978780copy number variation1nstd229human GRCh38 chr17: 39,015,790-39,330,652 , GRCh37.p13 chr17: 37,172,043-37,486,905 LOC105371768, PLXDC1, 13 more genes
    nsv6194483copy number variation1nstd214human GRCh38 chr17: 39,201,916-39,201,965 , GRCh37.p13 chr17: 37,358,169-37,358,218 RPL19
    nsv6133059copy number variation1nstd213human GRCh37 chr17: 37,070,000-37,430,001 , GRCh38.p12 chr17: 38,913,747-39,273,748 LASP1, ARL5C, 16 more genes
    nsv6133058copy number variation1nstd213human GRCh37 chr17: 37,070,000-37,420,001 , GRCh38.p12 chr17: 38,913,747-39,263,748 LASP1, ARL5C, 16 more genes
    nsv6133056copy number variation1nstd213human GRCh37 chr17: 36,400,000-39,740,001 , GRCh38.p12 chr17: 38,545,381-41,583,749 CACNB1, CDC6, 176 more genes
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5280924copy number variation1nstd204human GRCh38.p13 chr17: 39,129,801-39,494,000 , GRCh37.p13 chr17: 37,286,054-37,650,253 RPL19, TRC-GCA2-4, 11 more genes
    nsv4675728copy number variation1nstd102humanUncertain significance GRCh37 chr17: 37,323,328-37,551,861 , GRCh38.p12 chr17: 39,167,075-39,395,608 LOC105371768, RPL19, 5 more genes
    nsv4457831copy number variation1nstd102humanPathogenic GRCh37 chr17: 21,690,653-38,772,647 , GRCh38.p12 chr17: 22,164,047-40,616,395 LOC105371753, TAOK1, 474 more genes
    nsv4457589copy number variation1nstd102humanUncertain significance GRCh37 chr17: 37,190,609-37,868,002 , GRCh38.p12 chr17: 39,034,356-39,711,749 ERBB2, PGAP3, 23 more genes
    nsv4330632inversion1nstd166human GRCh37.p13 chr17: 18,838,526-72,042,289 , GRCh38.p12 chr17: 18,935,213-74,046,150 , ACACA, 1499 more genes
    nsv4262107copy number variation1nstd166human GRCh37.p13 chr17: 37,157,512-37,511,789 , GRCh38.p12 chr17: 39,001,259-39,355,536 LOC101929578, ARL5C, 13 more genes
    nsv3921422copy number variation1nstd102humanUncertain significance NCBI36 chr17: 34,563,112-34,695,553 , GRCh37.p13 chr17: 37,309,586-37,442,027 , GRCh38.p12 chr17: 39,153,333-39,285,774 LOC105371768, ARL5C, 7 more genes
    nsv3914783copy number variation1nstd102humanPathogenic NCBI36 chr17: 16,698,288-78,654,742 , GRCh37.p13 chr17: 16,757,563-81,048,189 , GRCh38.p12 chr17: 16,854,249-83,103,577 LOC105371922, GJD3, 1855 more genes
    nsv3914774copy number variation1nstd102humanLikely benign GRCh38 chr17: 39,036,037-39,694,679 , NCBI36 chr17: 34,445,816-35,104,458 , GRCh37 chr17: 37,192,290-37,850,932 CDK12, PNMT, 23 more genes
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