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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7093619copy number variation1nstd228human GRCh37 chr4: 171,508,974-190,957,473 , GRCh38.p12 chr4: 170,587,823-190,036,318 AGA, SLC25A4, 240 more genes
    nsv7056086inversion1nstd229human GRCh38 chr4: 174,912,619-184,252,538 , GRCh37.p13 chr4: 175,833,770-185,173,691 WDR17, LOC105377580, 84 more genes
    nsv7040070inversion1nstd229human GRCh38 chr4: 177,231,111-177,526,060 , GRCh37.p13 chr4: 178,152,265-178,447,214 RNA5SP172, AGA, 4 more genes
    nsv6755672copy number variation1nstd229human GRCh38 chr4: 177,338,183-177,343,857 , GRCh37.p13 chr4: 178,259,337-178,265,011 LOC105377558, NEIL3
    nsv6754861copy number variation1nstd229human GRCh38 chr4: 177,330,390-177,343,244 , GRCh37.p13 chr4: 178,251,544-178,264,398 NEIL3, LOC105377558
    nsv6753967copy number variation1nstd229human GRCh38 chr4: 177,175,194-177,385,830 , GRCh37.p13 chr4: 178,096,348-178,306,984 LOC105377558, LOC105377557, 2 more genes
    nsv6753732copy number variation1nstd229human GRCh38 chr4: 177,333,192-177,547,079 , GRCh37.p13 chr4: 178,254,346-178,468,233 LOC105377558, AGA, 3 more genes
    nsv6743842copy number variation1nstd229human GRCh38 chr4: 177,345,175-177,349,579 , GRCh37.p13 chr4: 178,266,329-178,270,733 NEIL3, LOC105377558
    nsv6743473copy number variation1nstd229human GRCh38 chr4: 177,325,901-177,424,600 , GRCh37.p13 chr4: 178,247,055-178,345,754 NEIL3, LOC105377558
    nsv6742177copy number variation1nstd229human GRCh38 chr4: 177,308,317-177,363,969 , GRCh37.p13 chr4: 178,229,471-178,285,123 LOC105377558, NEIL3
    nsv6740598copy number variation1nstd229human GRCh38 chr4: 177,318,312-177,634,231 , GRCh37.p13 chr4: 178,239,466-178,555,385 AGA-DT, NEIL3, 3 more genes
    nsv6740305copy number variation1nstd229human GRCh38 chr4: 177,316,985-177,540,328 , GRCh37.p13 chr4: 178,238,139-178,461,482 RNA5SP172, AGA, 3 more genes
    nsv6739637copy number variation1nstd229human GRCh38 chr4: 177,322,967-177,386,211 , GRCh37.p13 chr4: 178,244,121-178,307,365 NEIL3, LOC105377558
    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
    nsv6629590copy number variation1nstd224human GRCh37 chr4: 178,141,976-179,833,516 , GRCh38.p12 chr4: 177,220,822-178,912,362 AGA-DT, RNA5SP173, 14 more genes
    nsv6570050inversion1nstd223human GRCh38 chr4: 169,780,525-178,315,900 , GRCh37.p13 chr4: 170,701,676-179,237,054 LOC101928409, LOC100131553, 91 more genes
    nsv6388340copy number variation1nstd223human GRCh38 chr4: 177,344,701-177,349,300 , GRCh37.p13 chr4: 178,265,855-178,270,454 LOC105377558, NEIL3
    nsv6376117copy number variation1nstd223human GRCh38 chr4: 177,352,501-177,356,300 , GRCh37.p13 chr4: 178,273,655-178,277,454 LOC105377558, NEIL3
    nsv6315418copy number variation1nstd102humanUncertain significance GRCh37 chr4: 178,126,365-179,868,269 , GRCh38.p12 chr4: 177,205,211-178,947,115 AGA-DT, LINC01099, 14 more genes
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