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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097267copy number variation3nstd102humanUncertain significance GRCh37 chr5: 175,158,654-179,263,593 , GRCh38.p12 chr5: 175,731,651-179,836,593 LOC112267937, LMAN2, 122 more genes
    nsv7057944inversion1nstd229human GRCh38 chr5: 172,134,356-176,589,266 , GRCh37.p13 chr5: 171,561,360-176,016,267 MIR10523, NIFKP2, 92 more genes
    nsv7050002inversion1nstd229human GRCh38 chr5: 175,906,338-177,936,522 , GRCh37.p13 chr5: 175,333,341-177,363,523 PRR7, OR1X5P, 60 more genes
    nsv7041901inversion1nstd229human GRCh38 chr5: 175,920,087-179,128,938 , GRCh37.p13 chr5: 175,347,090-178,555,939 LOC100288803, NHP2, 98 more genes
    nsv7040659inversion1nstd229human GRCh38 chr5: 174,927,732-178,443,561 , GRCh37.p13 chr5: 174,354,735-177,870,562 RN7SKP148, FAM193B-DT, 90 more genes
    nsv7038290inversion1nstd229human GRCh38 chr5: 172,489,078-179,485,008 , GRCh37.p13 chr5: 171,916,082-178,912,009 ZFP2, NHP2, 168 more genes
    nsv6778400copy number variation1nstd229human GRCh38 chr5: 176,003,701-176,013,400 , GRCh37.p13 chr5: 175,430,704-175,440,403 THOC3, OR1X1P
    nsv6636326copy number variation1nstd102humanUncertain significance GRCh37 chr5: 175,343,531-175,477,274 , GRCh38.p12 chr5: 175,916,528-176,050,271 OR1X1P, THOC3, 2 more genes
    nsv6634369copy number variation1nstd102humanPathogenic GRCh37 chr5: 170,350,336-180,719,789 , GRCh38.p12 chr5: 170,923,332-181,292,788 GFPT2, FOXO1B, 287 more genes
    nsv6315448copy number variation1nstd102humanPathogenic GRCh37 chr5: 149,010,383-180,719,789 , GRCh38.p12 chr5: 149,630,820-181,292,788 GRM6, MIR1229, 554 more genes
    nsv6297671copy number variation1nstd186human GRCh37 chr5: 175,450,327-175,544,327 , GRCh38.p12 chr5: 176,023,324-176,117,324 THOC3, FAM153B, 1 more genes
    nsv6283520insertion1nstd214human GRCh38 chr5: 175,977,142-175,977,142 , GRCh37.p13 chr5: 175,404,145-175,404,145 THOC3-AS1, THOC3
    nsv6278907insertion2nstd214human GRCh38 chr5: 176,033,504-176,033,504 , GRCh37.p13 chr5: 175,460,507-175,460,507 THOC3
    nsv6277618insertion1nstd214human GRCh38 chr5: 175,977,174-175,977,174 , GRCh37.p13 chr5: 175,404,177-175,404,177 THOC3-AS1, THOC3
    nsv6172125copy number variation1nstd214human GRCh38 chr5: 176,031,097-176,031,148 , GRCh37.p13 chr5: 175,458,100-175,458,151 THOC3
    nsv6141281copy number variation1nstd206human GRCh38 chr5: 176,009,500-176,017,324 , GRCh37.p13 chr5: 175,436,503-175,444,327 THOC3
    nsv6141228copy number variation1nstd206human GRCh38 chr5: 176,031,324-176,044,324 , GRCh37.p13 chr5: 175,458,327-175,471,327 THOC3
    nsv6141201copy number variation1nstd206human GRCh38 chr5: 176,023,324-176,117,324 , GRCh37.p13 chr5: 175,450,327-175,544,327 THOC3, LOC100996385, 1 more genes
    nsv6140957copy number variation1nstd206human GRCh38 chr5: 175,988,000-176,015,324 , GRCh37.p13 chr5: 175,415,003-175,442,327 THOC3, OR1X1P
    nsv6140810copy number variation1nstd206human GRCh38 chr5: 175,965,193-176,002,000 , GRCh37.p13 chr5: 175,392,196-175,429,003 , THOC3-AS1, 1 more genes
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