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Items: 1 to 20 of 181

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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
    nsv5907231copy number variation1nstd209human GRCh38 chr5: 179,841,236-179,841,364 , GRCh37.p13 chr5: 179,268,236-179,268,364 MRNIP
    nsv5893628copy number variation1nstd209human GRCh38 chr5: 179,848,997-179,849,901 , GRCh37.p13 chr5: 179,275,997-179,276,901 MRNIP
    nsv5892664copy number variation1nstd209human GRCh38 chr5: 179,849,866-179,849,915 , GRCh37.p13 chr5: 179,276,866-179,276,915 MRNIP
    nsv5890816copy number variation1nstd209human GRCh38 chr5: 179,849,614-179,849,913 , GRCh37.p13 chr5: 179,276,614-179,276,913 MRNIP
    nsv5842260copy number variation2nstd209human GRCh38 chr5: 179,859,065-179,860,164 , GRCh37.p13 chr5: 179,286,065-179,287,164 MRNIP-DT, MRNIP, 1 more genes
    nsv5723726mobile element insertion1nstd211human GRCh38 chr5: 179,848,093-179,848,093 , GRCh37.p13 chr5: 179,275,093-179,275,093 MRNIP
    nsv5642992insertion1nstd207human GRCh38 chr5: 179,849,444-179,849,444 , GRCh37.p13 chr5: 179,276,444-179,276,444 MRNIP
    nsv5569486copy number variation1nstd207human GRCh38 chr5: 179,849,866-179,849,915 , GRCh37.p13 chr5: 179,276,866-179,276,915 MRNIP
    nsv5561640sequence alteration1nstd206human GRCh38 chr5: 179,554,688-180,310,132 , GRCh37.p13 chr5: 178,981,689-179,737,132 LTC4S, MIR340, 28 more genes
    nsv5537105insertion1nstd206human GRCh38 chr5: 179,855,855-179,855,904 , GRCh37.p13 chr5: 179,282,855-179,282,904 MRNIP
    nsv5470911copy number variation1nstd206human GRCh38 chr5: 179,849,006-179,849,842 , GRCh37.p13 chr5: 179,276,006-179,276,842 MRNIP
    nsv5456945copy number variation1nstd206human GRCh38 chr5: 179,853,549-179,869,825 , GRCh37.p13 chr5: 179,280,549-179,296,825 TBC1D9B, MRNIP-DT, 1 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
    nsv5319039copy number variation1nstd204human GRCh37.p13 chr5: 179,262,241-179,266,298 , GRCh38.p13 chr5: 179,835,241-179,839,298 SQSTM1, MRNIP
    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
    nsv5226230copy number variation1nstd204human GRCh38.p13 chr5: 179,835,010-179,839,237 , GRCh37.p13 chr5: 179,262,010-179,266,237 MRNIP, SQSTM1
    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
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