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Items: 1 to 20 of 130

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5561640sequence alteration1nstd206human GRCh38 chr5: 179,554,688-180,310,132 , GRCh37.p13 chr5: 178,981,689-179,737,132 LTC4S, MIR340, 28 more genes
    nsv5381440copy number variation1nstd102humanUncertain significance GRCh37 chr5: 178,699,902-179,263,603 , GRCh38.p12 chr5: 179,272,901-179,836,603 , GRCh38.p12 chr5|NW_016107298.1: 37,608-602,163 LOC105377762, LOC105377759, 21 more genes
    nsv5381377copy number variation1nstd102humanUncertain significance GRCh37 chr5: 178,770,758-179,263,603 , GRCh38.p12 chr5: 179,343,757-179,836,603 , GRCh38.p12 chr5|NW_016107298.1: 108,464-602,163 LOC100502572, C5orf60, 21 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
    nsv5233947copy number variation1nstd204human GRCh38.p13 chr5: 179,616,201-179,907,500 , GRCh37.p13 chr5: 179,043,202-179,334,500 CBY3, LOC100502572, 15 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
    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
    nsv4663016copy number variation1nstd186human GRCh37 chr5: 179,222,827-179,222,871 , GRCh38.p12 chr5: 179,795,826-179,795,870 , GRCh38.p12 chr5|NW_016107298.1: 561,403-561,447 LTC4S, MGAT4B
    nsv4597965copy number variation1nstd183human GRCh37 chr5: 179,222,827-179,222,940 , GRCh38.p12 chr5: 179,795,826-179,795,939 , GRCh38.p12 chr5|NW_016107298.1: 561,403-561,516 LTC4S, MGAT4B
    nsv4597964copy number variation1nstd183human GRCh37 chr5: 179,222,658-179,223,395 , GRCh38.p12 chr5: 179,795,657-179,796,394 , GRCh38.p12 chr5|NW_016107298.1: 561,234-561,971 MIR1229, MGAT4B, 1 more genes
    nsv4592952copy number variation2nstd183human GRCh37 chr5: 179,222,827-179,222,871 , GRCh38.p12 chr5: 179,795,826-179,795,870 , GRCh38.p12 chr5|NW_016107298.1: 561,403-561,447 MGAT4B, LTC4S
    nsv4590690copy number variation1nstd183human GRCh37 chr5: 179,218,857-179,222,997 , GRCh38.p12 chr5: 179,791,856-179,795,996 , GRCh38.p12 chr5|NW_016107298.1: 557,433-561,573 MGAT4B, LTC4S
    nsv4455758copy number variation1nstd102humanUncertain significance GRCh37 chr5: 179,180,782-179,231,973 , GRCh38.p12 chr5|NW_016107298.1: 519,377-570,546 , GRCh38.p12 chr5: 179,753,781-179,804,973 LOC100884169, MGAT4B, 4 more genes
    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
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