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Items: 1 to 20 of 97

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137216copy number variation1nstd102humanPathogenic GRCh37 chr17: 30,572,862-35,843,988 , GRCh38.p12 chr17: 32,245,843-36,446,544 PSMD11, C17orf50, 117 more genes
    nsv7095147copy number variation1nstd102humanUncertain significance GRCh37 chr17: 33,475,283-34,079,869 , GRCh38.p12 chr17: 35,148,264-35,752,850 SLC35G3, AP2B1, 26 more genes
    nsv7073998inversion1nstd229human GRCh38 chr17: 32,918,710-41,148,753 , GRCh37.p13 chr17: 31,245,728-39,305,005 LOC105371750, C17orf78, 298 more genes
    nsv6982202copy number variation1nstd229human GRCh38 chr17: 34,998,758-35,727,529 , GRCh37.p13 chr17: 33,325,777-34,034,851 SLFN11, LOC105371932, 32 more genes
    nsv6634448copy number variation1nstd102humanUncertain significance GRCh37 chr17: 33,756,756-34,005,513 , GRCh38.p12 chr17: 35,429,737-35,678,494 LOC100420062, TAF5LP1, 13 more genes
    nsv6511313copy number variation1nstd223human GRCh38 chr17: 35,570,087-35,574,100 , GRCh37.p13 chr17: 33,897,106-33,901,119 PEX12, SNHG30, 1 more genes
    nsv6499851copy number variation1nstd223human GRCh38 chr17: 34,998,758-35,727,531 , GRCh37.p13 chr17: 33,325,777-34,034,851 FNDC8, LOC101060119, 32 more genes
    nsv6133353copy number variation1nstd213human GRCh37 chr17: 33,210,000-34,670,001 , GRCh38.p12 chr17: 34,882,981-35,919,248 AP2B1, E2F3P1, 48 more genes
    nsv6133052copy number variation1nstd213human GRCh37 chr17: 33,850,000-34,430,001 , GRCh38.p12 chr17: 35,522,981-35,919,248 RASL10B, RDM1, 21 more genes
    nsv6133050copy number variation1nstd213human GRCh37 chr17: 32,790,000-34,510,001 , GRCh38.p12 chr17: 34,462,981-35,919,248 AP2B1, E2F3P1, 53 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
    nsv4762422inversion1nstd199human GRCh37 chr17: 151-36,202,676 , GRCh38.p12 chr17: 150,358-36,446,544 , ABR, 1046 more genes
    nsv4669043copy number variation1nstd186human GRCh37 chr17: 33,897,851-33,902,624 , GRCh38.p12 chr17: 35,570,832-35,575,605 PEX12, SNORD7, 1 more genes
    nsv4622769copy number variation2nstd183human GRCh37 chr17: 33,897,851-33,902,624 , GRCh38.p12 chr17: 35,570,832-35,575,605 PEX12, SNORD7, 1 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
    nsv4330632inversion1nstd166human GRCh37.p13 chr17: 18,838,526-72,042,289 , GRCh38.p12 chr17: 18,935,213-74,046,150 , ACACA, 1499 more genes
    nsv4233068copy number variation1nstd166human GRCh37.p13 chr17: 33,799,839-33,992,535 , GRCh38.p12 chr17: 35,472,820-35,665,516 , SNORD7, 11 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
    nsv3914031copy number variation1nstd102humanUncertain significance NCBI36 chr17: 30,480,991-31,118,181 , GRCh38 chr17: 35,129,859-35,767,049 , GRCh37 chr17: 33,456,878-34,094,068 UFM1P2, MMP28, 30 more genes
    nsv3907376copy number variation1nstd102humanUncertain significance GRCh37 chr17: 32,351,496-34,455,576 , GRCh38.p12 chr17: 34,024,477-35,919,248 CCL8, TAF5LP1, 67 more genes
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