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Items: 1 to 20 of 173

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5977361inversion1nstd209human GRCh38 chr7: 5,132,403-5,833,612 , GRCh37.p13 chr7: 5,172,034-5,873,243 , ACTB, 15 more genes
    nsv5954538insertion1nstd209human GRCh38 chr7: 5,671,805-5,671,805 , GRCh37.p13 chr7: 5,711,436-5,711,436 RNF216, RNF216-IT1
    nsv5693735mobile element insertion1nstd211human GRCh38 chr7: 5,666,419-5,666,419 , GRCh37.p13 chr7: 5,706,050-5,706,050 RNF216-IT1, RNF216
    nsv5562206sequence alteration1nstd206human GRCh38 chr7: 4,983,711-5,730,820 , GRCh37.p13 chr7: 5,023,342-5,770,451 , FSCN1, 21 more genes
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5554692sequence alteration1nstd206human GRCh38 chr7: 5,142,858-5,773,733 , GRCh37.p13 chr7: 5,182,489-5,813,364 , FSCN1, 14 more genes
    nsv5468254copy number variation1nstd206human GRCh38 chr7: 5,670,634-5,670,771 , GRCh37.p13 chr7: 5,710,265-5,710,402 RNF216, RNF216-IT1
    nsv5399306mobile element insertion1nstd206human GRCh38 chr7: 5,666,419-5,666,470 , GRCh37.p13 chr7: 5,706,050-5,706,101 RNF216, RNF216-IT1
    nsv4949924copy number variation1nstd200human GRCh38 chr7: 5,588,087-5,765,529 , GRCh37.p13 chr7: 5,627,718-5,805,160 , MIR6874, 3 more genes
    nsv4818581copy number variation1nstd200human GRCh37 chr7: 5,710,265-5,710,402 , GRCh38.p12 chr7: 5,670,634-5,670,771 RNF216-IT1, RNF216
    nsv4818577copy number variation1nstd200human GRCh37 chr7: 5,627,718-5,805,160 , GRCh38.p12 chr7: 5,588,087-5,765,529 , MIR6874, 3 more genes
    nsv4729029copy number variation1nstd102humanUncertain significance GRCh37 chr7: 5,676,440-5,965,440 , GRCh38.p12 chr7: 5,636,809-5,925,809 OCM, MIR6874, 6 more genes
    nsv4676029copy number variation1nstd102humanUncertain significance GRCh37 chr7: 5,702,085-5,949,898 , GRCh38.p12 chr7: 5,662,454-5,910,267 RNF216-IT1, CCZ1, 5 more genes
    nsv4675817copy number variation1nstd102humanPathogenic GRCh37 chr7: 1,648,373-10,627,513 , GRCh38.p12 chr7: 1,608,737-10,587,886 TTYH3, UNC93B2, 150 more genes
    nsv4604296copy number variation1nstd183human GRCh37 chr7: 5,706,219-5,769,489 , GRCh38.p12 chr7: 5,666,588-5,729,858 RNF216, RNF216-IT1, 1 more genes
    nsv4456827copy number variation1nstd102humanPathogenic GRCh37 chr7: 43,376-19,520,619 , GRCh38.p12 chr7: 43,376-19,480,996 MIR6836, EEF1A1P26, 277 more genes
    nsv4456094copy number variation1nstd102humanPathogenic GRCh37 chr7: 5,218,459-6,319,917 , GRCh38.p12 chr7: 5,178,828-6,280,286 MIR589, ACTB, 26 more genes
    nsv4455091copy number variation1nstd102humanPathogenic GRCh37 chr7: 10,365-159,119,707 , GRCh38.p12 chr7: 10,365-159,327,017 RPL23AP51, FLJ40288, 2684 more genes
    nsv4455055copy number variation1nstd102humanPathogenic GRCh37 chr7: 5,606,650-6,185,838 , GRCh38.p12 chr7: 5,567,019-6,146,207 RNF216, RNF216-IT1, 15 more genes
    nsv4366500copy number variation1nstd173human GRCh37 chr7: 5,682,409-5,856,074 , GRCh38.p12 chr7: 5,642,778-5,816,443 MIR6874, RNF216, 1 more genes
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