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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6130432mobile element insertion1nstd186human GRCh37 chr17: 61,845,773-61,845,824 , GRCh38.p12 chr17: 63,768,413-63,768,464 CCDC47
    nsv5944335copy number variation1nstd209human GRCh38 chr17: 63,749,135-63,749,481 , GRCh37.p13 chr17: 61,826,495-61,826,841 CCDC47
    nsv5941967copy number variation1nstd209human GRCh38 chr17: 63,747,984-63,748,118 , GRCh37.p13 chr17: 61,825,344-61,825,478 CCDC47
    nsv5938503copy number variation1nstd209human GRCh38 chr17: 63,763,611-63,763,714 , GRCh37.p13 chr17: 61,840,971-61,841,074 CCDC47
    nsv5730285mobile element insertion1nstd211human GRCh38 chr17: 63,768,413-63,768,413 , GRCh37.p13 chr17: 61,845,773-61,845,773 CCDC47
    nsv5697134mobile element insertion2nstd211human GRCh38 chr17: 63,771,063-63,771,063 , GRCh37.p13 chr17: 61,848,423-61,848,423 CCDC47
    nsv5658505insertion1nstd207human GRCh38 chr17: 63,768,396-63,768,396 , GRCh37.p13 chr17: 61,845,756-61,845,756 CCDC47
    nsv5600839copy number variation1nstd207human GRCh38 chr17: 63,747,984-63,748,118 , GRCh37.p13 chr17: 61,825,344-61,825,478 CCDC47
    nsv5600793copy number variation1nstd207human GRCh38 chr17: 63,763,613-63,763,718 , GRCh37.p13 chr17: 61,840,973-61,841,078 CCDC47
    nsv5598955copy number variation1nstd207human GRCh38 chr17: 63,759,508-63,759,559 , GRCh37.p13 chr17: 61,836,868-61,836,919 CCDC47
    nsv5554926mobile element insertion1nstd206human GRCh38 chr17: 63,768,413-63,768,464 , GRCh37.p13 chr17: 61,845,773-61,845,824 CCDC47
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5528770copy number variation1nstd206human GRCh38 chr17: 63,747,999-63,748,119 , GRCh37.p13 chr17: 61,825,359-61,825,479 CCDC47
    nsv5522960copy number variation1nstd206human GRCh38 chr17: 63,743,654-63,743,758 , GRCh37.p13 chr17: 61,821,014-61,821,118 CCDC47
    nsv5515544copy number variation1nstd206human GRCh38 chr17: 63,763,611-63,763,727 , GRCh37.p13 chr17: 61,840,971-61,841,087 CCDC47
    nsv5327334copy number variation1nstd204human GRCh38.p13 chr17: 63,747,989-63,748,128 , GRCh37.p13 chr17: 61,825,349-61,825,488 CCDC47
    nsv5292062copy number variation1nstd204human GRCh38.p13 chr17: 63,540,501-63,873,300 , GRCh37.p13 chr17: 61,617,862-61,950,660 , KCNH6, 18 more genes
    nsv5198956mobile element insertion1nstd203human GRCh38 chr17: 63,768,396-63,768,408 , GRCh37.p13 chr17: 61,845,756-61,845,768 CCDC47
    nsv5190835mobile element insertion1nstd203human GRCh38 chr17: 63,768,401-63,768,413 , GRCh37.p13 chr17: 61,845,761-61,845,773 CCDC47
    nsv5183548mobile element insertion1nstd203human GRCh38 chr17: 63,768,400-63,768,413 , GRCh37.p13 chr17: 61,845,760-61,845,773 CCDC47
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