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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7057296inversion1nstd229human GRCh38 chr4: 168,056,716-168,486,346 , GRCh37.p13 chr4: 168,977,867-169,407,497 DDX60L, ANXA10, 2 more genes
    nsv7057058inversion1nstd229human GRCh38 chr4: 165,065,528-168,877,636 , GRCh37.p13 chr4: 165,986,680-169,798,787 DDX60L, RNA5SP170, 33 more genes
    nsv7056217inversion1nstd229human GRCh38 chr4: 166,607,935-172,500,612 , GRCh37.p13 chr4: 167,529,086-173,421,763 DDX60, LOC105377529, 50 more genes
    nsv7042913inversion1nstd229human GRCh38 chr4: 167,282,036-168,440,434 , GRCh37.p13 chr4: 168,203,187-169,361,585 DDX60, DDX60L, 6 more genes
    nsv6755716copy number variation1nstd229human GRCh38 chr4: 168,153,259-168,219,126 , GRCh37.p13 chr4: 169,074,410-169,140,277 LOC105377524, DDX60, 1 more genes
    nsv6754614copy number variation1nstd229human GRCh38 chr4: 168,033,958-168,091,372 , GRCh37.p13 chr4: 168,955,109-169,012,523 ANXA10, LOC105377523
    nsv6752902copy number variation1nstd229human GRCh38 chr4: 167,572,007-168,851,753 , GRCh37.p13 chr4: 168,493,158-169,772,904 RPL9P16, PALLD, 11 more genes
    nsv6751150copy number variation1nstd229human GRCh38 chr4: 168,144,636-168,158,022 , GRCh37.p13 chr4: 169,065,787-169,079,173 ANXA10
    nsv6751109copy number variation1nstd229human GRCh38 chr4: 168,176,119-168,182,414 , GRCh37.p13 chr4: 169,097,270-169,103,565 LOC105377524, ANXA10
    nsv6750486copy number variation1nstd229human GRCh38 chr4: 168,161,501-168,168,900 , GRCh37.p13 chr4: 169,082,652-169,090,051 ANXA10, LOC105377524
    nsv6750122copy number variation1nstd229human GRCh38 chr4: 168,153,434-168,153,471 , GRCh37.p13 chr4: 169,074,585-169,074,622 ANXA10
    nsv6750073copy number variation1nstd229human GRCh38 chr4: 168,143,601-168,162,100 , GRCh37.p13 chr4: 169,064,752-169,083,251 ANXA10
    nsv6747972copy number variation1nstd229human GRCh38 chr4: 168,036,260-168,093,292 , GRCh37.p13 chr4: 168,957,411-169,014,443 LOC105377523, ANXA10
    nsv6745088copy number variation1nstd229human GRCh38 chr4: 168,139,515-168,236,465 , GRCh37.p13 chr4: 169,060,666-169,157,616 LOC105377524, ANXA10, 1 more genes
    nsv6744847copy number variation1nstd229human GRCh38 chr4: 168,102,478-168,102,859 , GRCh37.p13 chr4: 169,023,629-169,024,010 ANXA10
    nsv6744799copy number variation1nstd229human GRCh38 chr4: 168,151,534-168,163,940 , GRCh37.p13 chr4: 169,072,685-169,085,091 ANXA10
    nsv6742415copy number variation1nstd229human GRCh38 chr4: 167,972,714-168,331,253 , GRCh37.p13 chr4: 168,893,865-169,252,404 LOC105377524, LOC105377523, 2 more genes
    nsv6738949copy number variation1nstd229human GRCh38 chr4: 167,960,180-168,093,349 , GRCh37.p13 chr4: 168,881,331-169,014,500 ANXA10, LOC105377523
    nsv6634364copy number variation1nstd102humanPathogenic GRCh37 chr4: 167,779,888-190,957,473 , GRCh38.p12 chr4: 166,858,737-190,036,318 LOC101928551, LOC107986330, 279 more genes
    nsv6634351copy number variation1nstd102humanPathogenic GRCh37 chr4: 159,174,483-190,957,473 , GRCh38.p12 chr4: 158,253,331-190,036,318 COPS3P1, LOC339975, 363 more genes
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