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Items: 1 to 20 of 108

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5976694inversion1nstd209human GRCh38 chr5: 179,854,164-180,408,925 , GRCh37.p13 chr5: 179,281,164-179,835,925 MAPK9, GFPT2, 11 more genes
    nsv5631804insertion1nstd207human GRCh38 chr5: 180,015,571-180,015,571 , GRCh37.p13 chr5: 179,442,571-179,442,571 RNF130, MIR340
    nsv5574017copy number variation1nstd207human GRCh38 chr5: 180,015,619-180,015,745 , GRCh37.p13 chr5: 179,442,619-179,442,745 MIR340, RNF130
    nsv5561640sequence alteration1nstd206human GRCh38 chr5: 179,554,688-180,310,132 , GRCh37.p13 chr5: 178,981,689-179,737,132 LTC4S, MIR340, 28 more genes
    nsv5301596copy number variation1nstd204human GRCh38.p13 chr5: 179,616,292-180,442,361 , GRCh37.p13 chr5: 179,043,293-179,869,361 MIR1229, MAPK9, 25 more genes
    nsv5229540copy number variation1nstd204human GRCh38.p13 chr5: 179,907,701-180,437,500 , GRCh37.p13 chr5: 179,334,701-179,864,500 RPS15AP18, LOC646058, 9 more genes
    nsv4949296copy number variation1nstd200human GRCh38 chr5: 179,752,913-180,268,215 , GRCh37.p13 chr5: 179,179,914-179,695,215 MIR1229, MAPK9, 17 more genes
    nsv4828418copy number variation1nstd200human GRCh37 chr5: 179,179,914-179,695,214 , GRCh38.p12 chr5: 179,752,913-180,268,214 LOC100884169, MGAT4B, 17 more genes
    nsv4768375copy number variation1nstd102humanPathogenic GRCh37 chr5: 170,805,664-180,719,789 , GRCh38.p12 chr5: 171,378,660-181,292,788 LINC01863, PRDX2P3, 279 more genes
    nsv4765150insertion1nstd199human GRCh37 chr5: 179,442,562-179,442,562 , GRCh38.p12 chr5: 180,015,562-180,015,562 RNF130, MIR340
    nsv4675130copy number variation1nstd102humanUncertain significance GRCh37 chr5: 178,487,249-180,622,216 , GRCh38.p12 chr5: 179,060,248-181,195,216 OR2V2, TRV-AAC1-2, 81 more genes
    nsv4597966copy number variation1nstd183human GRCh37 chr5: 179,402,769-179,806,356 , GRCh38.p12 chr5: 179,975,769-180,379,356 MAPK9, GFPT2, 6 more genes
    nsv4522666copy number variation1nstd166human GRCh37.p13 chr5: 179,401,999-179,468,000 , GRCh38.p12 chr5: 179,974,999-180,041,000 RNF130, MIR340
    nsv4455497copy number variation1nstd102humanPathogenic GRCh37 chr5: 176,848,982-180,719,789 , GRCh38.p12 chr5: 177,421,981-181,292,788 HEIH, MGAT4B, 149 more genes
    nsv4436723copy number variation1nstd102humanUncertain significance GRCh37 chr5: 179,065,654-179,541,490 , GRCh38.p12 chr5: 179,638,653-180,114,490 , GRCh38.p12 chr5|NW_016107298.1: 420,871-673,059 LOC646058, RN7SKP150, 20 more genes
    nsv4350559copy number variation1nstd102humanPathogenic GRCh37 chr5: 174,990,352-180,690,937 , GRCh38.p12 chr5: 175,563,349-181,263,936 FAF2, ARL10, 198 more genes
    nsv4350315copy number variation1nstd102humanLikely pathogenic GRCh37 chr5: 177,776,148-180,687,012 , GRCh38.p12 chr5: 178,349,147-181,260,011 CANX, FOXO1B, 114 more genes
    nsv4347913copy number variation1nstd102humanLikely pathogenic GRCh37 chr5: 175,843,728-180,703,728 , GRCh38.p12 chr5: 176,416,727-181,276,727 CANX, CLTB, 177 more genes
    nsv4125953copy number variation1nstd166human GRCh37.p13 chr5: 179,398,727-179,591,758 , GRCh38.p12 chr5: 179,971,727-180,164,758 LOC646058, MIR340, 2 more genes
    nsv4125210copy number variation1nstd166human GRCh37.p13 chr5: 179,103,531-180,092,516 , GRCh38.p12 chr5: 179,676,530-180,665,516 LOC100329129, MIR1229, 27 more genes
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