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Items: 1 to 20 of 219

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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
    nsv7076052inversion1nstd229human GRCh38 chr17: 34,741,220-35,013,198 , GRCh37.p13 chr17: 33,068,239-33,340,217 LIG3, RAD51L3-RFFL, 5 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
    nsv6997643copy number variation1nstd229human GRCh38 chr17: 34,956,129-34,965,838 , GRCh37.p13 chr17: 33,283,148-33,292,857 ZNF830, CCT6B
    nsv6991987copy number variation1nstd229human GRCh38 chr17: 34,374,301-34,929,500 , GRCh37.p13 chr17: 32,701,320-33,256,519 TMEM132E, TMEM132E-DT, 5 more genes
    nsv6989194copy number variation1nstd229human GRCh38 chr17: 34,963,555-34,967,899 , GRCh37.p13 chr17: 33,290,574-33,294,918 CCT6B, ZNF830
    nsv6981726copy number variation1nstd229human GRCh38 chr17: 34,959,348-34,982,808 , GRCh37.p13 chr17: 33,286,367-33,309,827 LIG3, ZNF830, 1 more genes
    nsv6591124inversion1nstd223human GRCh38 chr17: 34,957,183-34,958,249 , GRCh37.p13 chr17: 33,284,202-33,285,268 CCT6B
    nsv6587462inversion1nstd223human GRCh38 chr17: 34,932,834-34,934,031 , GRCh37.p13 chr17: 33,259,853-33,261,050 CCT6B
    nsv6586658inversion1nstd223human GRCh38 chr17: 34,953,482-34,953,924 , GRCh37.p13 chr17: 33,280,501-33,280,943 CCT6B
    nsv6581207inversion1nstd223human GRCh38 chr17: 34,938,084-34,938,446 , GRCh37.p13 chr17: 33,265,103-33,265,465 CCT6B
    nsv6497486copy number variation1nstd223human GRCh38 chr17: 34,547,647-35,364,191 , GRCh37.p13 chr17: 32,874,666-33,691,210 LOC105371742, ZNF830, 19 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
    nsv6133352copy number variation1nstd213human GRCh37 chr17: 33,070,000-33,260,001 , GRCh38.p12 chr17: 34,742,981-34,932,982 CCT6B, LOC105371742
    nsv6133051copy number variation1nstd213human GRCh37 chr17: 33,000,000-33,420,001 , GRCh38.p12 chr17: 34,672,981-35,092,982 LIG3, RAD51D, 8 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
    nsv6087193insertion1nstd212human GRCh38 chr17: 34,977,741-34,977,741 , GRCh37.p13 chr17: 33,304,760-33,304,760 CCT6B
    nsv6040230copy number variation1nstd212human GRCh38 chr17: 34,977,692-34,977,925 , GRCh37.p13 chr17: 33,304,711-33,304,944 CCT6B
    nsv5939374copy number variation1nstd209human GRCh38 chr17: 34,930,510-34,931,119 , GRCh37.p13 chr17: 33,257,529-33,258,138 CCT6B
    nsv5645143insertion1nstd207human GRCh38 chr17: 34,977,736-34,977,736 , GRCh37.p13 chr17: 33,304,755-33,304,755 CCT6B
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