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Items: 1 to 20 of 146

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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
    nsv7067347inversion1nstd229human GRCh38 chr17: 40,703,588-40,707,985 , GRCh37.p13 chr17: 38,859,840-38,864,237 KRT24
    nsv7066102inversion1nstd229human GRCh38 chr17: 40,703,479-40,712,349 , GRCh37.p13 chr17: 38,859,731-38,868,601 KRT24
    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
    nsv6984452copy number variation1nstd229human GRCh38 chr17: 40,685,152-40,733,498 , GRCh37.p13 chr17: 38,841,404-38,889,750 KRT223P, LOC105371775, 1 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
    nsv6514015copy number variation1nstd223human GRCh38 chr17: 40,682,883-40,699,164 , GRCh37.p13 chr17: 38,839,135-38,855,416 KRT24, LOC105371775
    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
    nsv5341713translocation1nstd200human GRCh37 chr17: 38,850,381-38,850,381 , GRCh37 chr17: 38,850,476-38,850,476 , GRCh38.p12 chr17: 40,694,129-40,694,129 , GRCh38.p12 chr17: 40,694,224-40,694,224 KRT24, LOC105371775
    nsv5013693copy number variation1nstd200human GRCh38 chr17: 40,682,814-40,699,207 , GRCh37.p13 chr17: 38,839,066-38,855,459 LOC105371775, KRT24
    nsv4864649copy number variation1nstd200human GRCh37 chr17: 38,839,066-38,855,459 , GRCh38.p12 chr17: 40,682,814-40,699,207 LOC105371775, KRT24
    nsv4679355copy number variation1nstd189human GRCh37.p13 chr17: 38,659,900-39,414,647 , GRCh38.p12 chr17: 40,503,648-41,258,395 , CCR7, 54 more genes
    nsv4365890copy number variation1nstd173human GRCh37 chr17: 38,846,470-38,880,294 , GRCh38.p12 chr17: 40,690,218-40,724,042 LOC105371775, KRT24, 1 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
    nsv4265791copy number variation1nstd166human GRCh37.p13 chr17: 38,849,503-38,849,707 , GRCh38.p12 chr17: 40,693,251-40,693,455 LOC105371775, KRT24
    nsv4253252copy number variation1nstd166human GRCh37.p13 chr17: 38,839,144-38,855,417 , GRCh38.p12 chr17: 40,682,892-40,699,165 LOC105371775, KRT24
    nsv3948881copy number variation1nstd167human GRCh37 chr17: 38,857,996-38,858,028 , GRCh38.p12 chr17: 40,701,744-40,701,776 KRT24
    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
    nsv3913552copy number variation1nstd102humanPathogenic GRCh38 chr17: 36,449,220-75,053,130 , NCBI36 chr17: 54,950,518-70,560,820 , GRCh37 chr17: 57,595,736-73,049,225 RNU6-131P, ZNF652, 1075 more genes
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