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Items: 1 to 20 of 228

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7066656inversion1nstd229human GRCh38 chr17: 40,822,205-41,582,529 , GRCh37.p13 chr17: 38,978,457-39,738,781 LOC105371777, KRT10, 69 more genes
    nsv6992915copy number variation1nstd229human GRCh38 chr17: 41,383,458-41,402,096 , GRCh37.p13 chr17: 39,539,710-39,558,348 LOC100505782, KRT31, 1 more genes
    nsv6987154copy number variation1nstd229human GRCh38 chr17: 41,277,005-41,430,682 , GRCh37.p13 chr17|NW_003315953.1: 16,589-119,548 , GRCh37.p13 chr17: 39,433,257-39,586,934 TBC1D3P7, KRT41P, 11 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
    nsv6624275copy number variation1nstd224human GRCh37 chr17: 39,525,970-39,538,623 , GRCh38.p12 chr17: 41,369,718-41,382,371 KRT34, KRT33B
    nsv6509819copy number variation1nstd223human GRCh38 chr17: 41,381,201-41,382,900 , GRCh37.p13 chr17: 39,537,453-39,539,152 KRT34
    nsv6507182copy number variation1nstd223human GRCh38 chr17: 41,369,559-41,382,000 , GRCh37.p13 chr17: 39,525,811-39,538,252 KRT33B, KRT34
    nsv6504427copy number variation1nstd223human GRCh38 chr17: 41,277,005-41,430,682 , GRCh37.p13 chr17|NW_003315953.1: 16,589-119,548 , GRCh37.p13 chr17: 39,433,257-39,586,934 KRTAP16-1, TBC1D3P7, 11 more genes
    nsv6504032copy number variation1nstd223human GRCh38 chr17: 41,379,201-41,383,000 , GRCh37.p13 chr17: 39,535,453-39,539,252 KRT34
    nsv6501693copy number variation1nstd223human GRCh38 chr17: 41,379,456-41,395,148 , GRCh37.p13 chr17: 39,535,708-39,551,400 KRT34, KRT31
    nsv6306994copy number variation1nstd186human GRCh37 chr17: 39,531,967-39,539,374 , GRCh38.p12 chr17: 41,375,715-41,383,122 KRT34
    nsv6145882copy number variation1nstd206human GRCh38 chr17: 41,375,674-41,383,149 , GRCh37.p13 chr17: 39,531,926-39,539,401 KRT34
    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
    nsv6034433copy number variation1nstd212human GRCh38 chr17: 41,375,998-41,383,306 , GRCh37.p13 chr17: 39,532,250-39,539,558 KRT34
    nsv5947431copy number variation1nstd209human GRCh38 chr17: 41,375,715-41,383,024 , GRCh37.p13 chr17: 39,531,967-39,539,276 KRT34
    nsv5874864copy number variation1nstd209human GRCh38 chr17: 41,375,189-41,383,142 , GRCh37.p13 chr17: 39,531,441-39,539,394 KRT34
    nsv5651024insertion1nstd207human GRCh38 chr17: 41,378,529-41,378,529 , GRCh37.p13 chr17: 39,534,781-39,534,781 KRT34
    nsv5645870insertion1nstd207human GRCh38 chr17: 41,379,698-41,379,698 , GRCh37.p13 chr17: 39,535,950-39,535,950 KRT34
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
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