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Items: 1 to 20 of 371

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094421copy number variation1nstd102humanUncertain significance GRCh37 chr14: 21,671,278-22,005,055 , GRCh38.p12 chr14: 21,203,119-21,536,921 RN7SL650P, SNORD9, 14 more genes
    nsv7094244copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,915,399-22,005,055 , GRCh38.p12 chr14: 20,447,240-21,536,921 ARHGEF40, LOC105370398, 78 more genes
    nsv7072621inversion1nstd229human GRCh38 chr14: 20,991,576-21,885,954 , GRCh37.p13 chr14: 21,459,735-22,354,136 LINC00641, TRAV13-1, 61 more genes
    nsv7067406inversion1nstd229human GRCh38 chr14: 21,243,110-21,243,156 , GRCh37.p13 chr14: 21,711,269-21,711,315 HNRNPC
    nsv7059593inversion1nstd229human GRCh38 chr14: 21,238,320-21,375,314 , GRCh37.p13 chr14: 21,706,479-21,843,473 MRPS17P6, RPGRIP1, 2 more genes
    nsv7058177inversion1nstd229human GRCh38 chr14: 21,098,135-21,342,114 , GRCh37.p13 chr14: 21,566,294-21,810,273 RNU6-252P, ZNF219, 11 more genes
    nsv6954607copy number variation1nstd229human GRCh38 chr14: 21,218,791-21,220,888 , GRCh37.p13 chr14: 21,686,950-21,689,047 HNRNPC
    nsv6952001copy number variation1nstd229human GRCh38 chr14: 21,213,939-21,218,329 , GRCh37.p13 chr14: 21,682,098-21,686,488 HNRNPC
    nsv6950872copy number variation1nstd229human GRCh38 chr14: 21,250,937-21,253,028 , GRCh37.p13 chr14: 21,719,096-21,721,187 HNRNPC
    nsv6949539copy number variation1nstd229human GRCh38 chr14: 21,223,039-21,342,016 , GRCh37.p13 chr14: 21,691,198-21,810,175 HNRNPC, MRPS17P6, 1 more genes
    nsv6948562copy number variation1nstd229human GRCh38 chr14: 21,234,845-21,234,890 , GRCh37.p13 chr14: 21,703,004-21,703,049 HNRNPC
    nsv6948170copy number variation1nstd229human GRCh38 chr14: 21,209,692-21,210,180 , GRCh37.p13 chr14: 21,677,851-21,678,339 HNRNPC
    nsv6945924copy number variation1nstd229human GRCh38 chr14: 21,211,381-21,450,257 , GRCh37.p13 chr14: 21,679,540-21,918,416 EIF4EBP1P1, RPGRIP1, 9 more genes
    nsv6943911copy number variation1nstd229human GRCh38 chr14: 21,222,372-21,227,292 , GRCh37.p13 chr14: 21,690,531-21,695,451 HNRNPC
    nsv6942207copy number variation1nstd229human GRCh38 chr14: 21,241,420-21,245,759 , GRCh37.p13 chr14: 21,709,579-21,713,918 HNRNPC
    nsv6941179copy number variation1nstd229human GRCh38 chr14: 21,203,821-21,230,003 , GRCh37.p13 chr14: 21,671,980-21,698,162 HNRNPC, LINC00641
    nsv6637860copy number variation1nstd102humanUncertain significance GRCh37 chr14: 21,496,133-21,962,265 , GRCh38.p12 chr14: 21,027,974-21,494,106 ARHGEF40, RN7SL650P, 28 more genes
    nsv6637318copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,690,196-23,114,522 , GRCh38.p12 chr14: 20,222,037-22,645,313 TRAJ21, TRAJ44, 239 more genes
    nsv6588092inversion1nstd223human GRCh38 chr14: 21,232,390-21,232,930 , GRCh37.p13 chr14: 21,700,549-21,701,089 HNRNPC
    nsv6581430inversion1nstd223human GRCh38 chr14: 21,228,639-21,228,877 , GRCh37.p13 chr14: 21,696,798-21,697,036 HNRNPC
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