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Items: 1 to 20 of 196

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098935copy number variation1nstd102humanUncertain significance GRCh38 chr17: 43,603,558-44,033,313 , GRCh37.p13 chr17: 41,680,926-42,110,681 LOC107985086, MPP2, 21 more genes
    nsv7074724inversion1nstd229human GRCh38 chr17: 43,776,961-43,784,837 , GRCh37.p13 chr17: 41,854,329-41,862,205 CFAP97D1, DUSP3
    nsv7059088inversion1nstd229human GRCh38 chr17: 43,771,429-43,771,495 , GRCh37.p13 chr17: 41,848,797-41,848,863 DUSP3
    nsv6991508copy number variation1nstd229human GRCh38 chr17: 42,821,629-43,873,068 , GRCh37.p13 chr17: 40,973,647-41,950,436 RND2, LOC107985077, 50 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
    nsv6978937copy number variation1nstd229human GRCh38 chr17: 43,735,120-43,806,192 , GRCh37.p13 chr17: 41,812,488-41,883,560 MPP3, DUSP3, 2 more genes
    nsv6512830copy number variation1nstd223human GRCh38 chr17: 43,770,401-43,772,200 , GRCh37.p13 chr17: 41,847,769-41,849,568 DUSP3
    nsv6496804copy number variation1nstd223human GRCh38 chr17: 43,756,375-43,767,241 , GRCh37.p13 chr17: 41,833,743-41,844,609 SOST, DUSP3
    nsv6314057copy number variation1nstd102humanUncertain significance GRCh37 chr17: 41,202,796-41,974,964 , GRCh38.p12 chr17: 43,050,779-43,897,596 TMEM106A, MPP2, 33 more genes
    nsv6271455copy number variation1nstd214human GRCh38 chr17: 43,768,680-43,768,730 , GRCh37.p13 chr17: 41,846,048-41,846,098 DUSP3
    nsv5934284copy number variation1nstd209human GRCh38 chr17: 43,768,680-43,768,730 , GRCh37.p13 chr17: 41,846,048-41,846,098 DUSP3
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5526908copy number variation1nstd206human GRCh38 chr17: 43,732,488-43,774,082 , GRCh37.p13 chr17: 41,809,856-41,851,450 DUSP3, SOST
    nsv5513968copy number variation1nstd206human GRCh38 chr17: 43,770,421-43,771,737 , GRCh37.p13 chr17: 41,847,789-41,849,105 DUSP3
    nsv5392789copy number variation1nstd186human GRCh37 chr17: 41,847,789-41,849,104 , GRCh38.p12 chr17: 43,770,421-43,771,736 DUSP3
    nsv5358882translocation1nstd200human GRCh38 chr17: 43,770,421-43,770,421 , GRCh38 chr17: 43,771,735-43,771,735 , GRCh37.p13 chr17: 41,849,103-41,849,103 , GRCh37.p13 chr17: 41,847,789-41,847,789 DUSP3
    nsv5324249copy number variation1nstd204human GRCh38.p13 chr17: 43,770,420-43,771,735 , GRCh37.p13 chr17: 41,847,788-41,849,103 DUSP3
    nsv5290641copy number variation1nstd204human GRCh38.p13 chr17: 43,770,401-43,771,700 , GRCh37.p13 chr17: 41,847,769-41,849,068 DUSP3
    nsv5285628copy number variation1nstd204human GRCh38.p13 chr17: 43,770,390-43,771,772 , GRCh37.p13 chr17: 41,847,758-41,849,140 DUSP3
    nsv5281388copy number variation1nstd204human GRCh38.p13 chr17: 43,769,690-43,771,672 , GRCh37.p13 chr17: 41,847,058-41,849,040 DUSP3
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