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Items: 1 to 20 of 205

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095150copy number variation1nstd102humanUncertain significance GRCh37 chr17: 37,821,613-38,458,253 , GRCh38.p12 chr17: 39,665,360-40,302,001 ZPBP2, MED24, 28 more genes
    nsv7075890inversion1nstd229human GRCh38 chr17: 40,026,853-40,035,780 , GRCh37.p13 chr17: 38,183,106-38,192,033 MED24, SNORD124, 1 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
    nsv6988739copy number variation1nstd229human GRCh38 chr17: 40,019,850-40,021,953 , GRCh37.p13 chr17: 38,176,103-38,178,206 MED24
    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
    nsv6983090copy number variation1nstd229human GRCh38 chr17: 40,018,328-40,037,472 , GRCh37.p13 chr17: 38,174,581-38,193,725 SNORD124, MIR6884, 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
    nsv6593494inversion1nstd223human GRCh38 chr17: 40,047,520-40,047,943 , GRCh37.p13 chr17: 38,203,773-38,204,196 MED24
    nsv6576223inversion1nstd223human GRCh38 chr17: 40,049,697-40,050,150 , GRCh37.p13 chr17: 38,205,950-38,206,403 MED24
    nsv6510794copy number variation1nstd223human GRCh38 chr17: 40,040,140-40,047,791 , GRCh37.p13 chr17: 38,196,393-38,204,044 MED24
    nsv6500112copy number variation1nstd223human GRCh38 chr17: 40,044,601-40,047,600 , GRCh37.p13 chr17: 38,200,854-38,203,853 MED24
    nsv6496616copy number variation1nstd223human GRCh38 chr17: 40,019,850-40,021,942 , GRCh37.p13 chr17: 38,176,103-38,178,195 MED24
    nsv6496579copy number variation1nstd223human GRCh38 chr17: 40,040,178-40,040,793 , GRCh37.p13 chr17: 38,196,431-38,197,046 MED24
    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
    nsv6027573copy number variation1nstd212human GRCh38 chr17: 40,046,133-40,046,290 , GRCh37.p13 chr17: 38,202,386-38,202,543 MED24
    nsv5971902insertion1nstd209human GRCh38 chr17: 40,043,885-40,043,885 , GRCh37.p13 chr17: 38,200,138-38,200,138 MED24
    nsv5942084copy number variation1nstd209human GRCh38 chr17: 40,040,030-40,040,323 , GRCh37.p13 chr17: 38,196,283-38,196,576 MED24
    nsv5927580copy number variation1nstd209human GRCh38 chr17: 40,049,997-40,050,395 , GRCh37.p13 chr17: 38,206,250-38,206,648 MED24
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5518547copy number variation1nstd206human GRCh38 chr17: 40,043,637-40,044,630 , GRCh37.p13 chr17: 38,199,890-38,200,883 MED24
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