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Items: 1 to 20 of 99

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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
    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
    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
    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
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5149816mobile element insertion1nstd203human GRCh38 chr17: 34,963,853-34,963,870 , GRCh37.p13 chr17: 33,290,872-33,290,889 CCT6B, ZNF830
    nsv5029046copy number variation1nstd200human GRCh38 chr17: 34,959,348-34,982,808 , GRCh37.p13 chr17: 33,286,367-33,309,827 ZNF830, LIG3, 1 more genes
    nsv4762422inversion1nstd199human GRCh37 chr17: 151-36,202,676 , GRCh38.p12 chr17: 150,358-36,446,544 , ABR, 1046 more genes
    nsv4675860copy number variation1nstd102humanUncertain significance GRCh37 chr17: 33,073,917-33,863,479 , GRCh38.p12 chr17: 34,746,898-35,536,460 RPL37P22, LIG3, 26 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
    nsv4436271copy number variation1nstd102humanUncertain significance GRCh37 chr17: 31,889,285-33,557,612 , GRCh38.p12 chr17: 33,562,266-35,230,593 LOC105371739, CCL7, 33 more genes
    nsv4384972copy number variation1nstd173human GRCh37 chr17: 27,710,978-33,392,085 , GRCh38.p12 chr17: 29,383,960-35,065,066 , LOC105371737, 137 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
    nsv4234046copy number variation1nstd166human GRCh37.p13 chr17: 30,657,307-33,838,598 , GRCh38.p12 chr17: 32,330,288-35,511,579 , PSMD11, 65 more genes
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