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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148156copy number variation1nstd102humanPathogenic GRCh38 chr6: 161,349,282-170,584,790 , GRCh37.p13 chr6: 161,770,314-170,893,878 LOC105378126, LOC107986550, 149 more genes
    nsv7137133copy number variation1nstd102humanUncertain significance GRCh37 chr6: 159,006,336-170,713,678 , GRCh38.p12 chr6: 158,585,304-170,404,590 LOC101929460, GPR31, 199 more genes
    nsv7052981inversion1nstd229human GRCh38 chr6: 167,557,448-168,005,975 , GRCh37.p13 chr6: 168,042,074-168,406,655 LINC01558, LOC105378130, 12 more genes
    nsv7051730inversion1nstd229human GRCh38 chr6: 167,665,486-170,032,054 , GRCh37.p13 chr6: 168,066,166-170,347,278 WDR27, KIF25, 49 more genes
    nsv7045607inversion1nstd229human GRCh38 chr6: 167,962,412-169,542,840 , GRCh37.p13 chr6: 168,363,092-169,942,936 LOC105378137, LOC105378140, 30 more genes
    nsv7038888inversion1nstd229human GRCh38 chr6: 167,222,887-168,363,767 , GRCh37.p13 chr6: 167,636,375-168,764,447 LOC101929420, LOC102724220, 32 more genes
    nsv6816889copy number variation1nstd229human GRCh38 chr6: 167,932,865-168,197,071 , GRCh37.p13 chr6: 168,333,545-168,597,751 LOC107986673, KIF25-AS1, 6 more genes
    nsv6815680copy number variation1nstd229human GRCh38 chr6: 167,970,152-168,127,973 , GRCh37.p13 chr6: 168,370,832-168,528,653 KIF25, HGC6.3, 5 more genes
    nsv6814614copy number variation1nstd229human GRCh38 chr6: 167,976,185-167,976,568 , GRCh37.p13 chr6: 168,376,865-168,377,248 HGC6.3
    nsv6802899copy number variation1nstd229human GRCh38 chr6: 167,862,320-168,095,911 , GRCh37.p13 chr6: 168,263,000-168,496,591 LOC105378135, FRMD1, 5 more genes
    nsv6799877copy number variation1nstd229human GRCh38 chr6: 167,939,249-168,228,718 , GRCh37.p13 chr6: 168,339,929-168,629,398 LOC107986548, KIF25-AS1, 7 more genes
    nsv6636689copy number variation1nstd102humanPathogenic GRCh37 chr6: 163,181,847-170,919,482 , GRCh38.p12 chr6: 162,760,815-170,610,394 GNG5P1, LINC01558, 144 more genes
    nsv6634373copy number variation1nstd102humanPathogenic GRCh37 chr6: 163,836,226-170,893,669 , GRCh38.p12 chr6: 163,415,194-170,584,581 LOC107986547, LOC107986550, 132 more genes
    nsv6631221copy number variation2nstd224human GRCh37 chr6: 168,362,683-168,597,599 , GRCh38.p12 chr6: 167,962,003-168,196,919 KIF25, AFDN, 5 more genes
    nsv6631220copy number variation1nstd224human GRCh37 chr6: 168,352,586-168,597,242 , GRCh38.p12 chr6: 167,951,906-168,196,562 KIF25, AFDN, 5 more genes
    nsv6631219copy number variation1nstd224human GRCh37 chr6: 168,352,445-168,599,333 , GRCh38.p12 chr6: 167,951,765-168,198,653 KIF25, AFDN, 5 more genes
    nsv6631218copy number variation1nstd224human GRCh37 chr6: 168,348,559-168,609,335 , GRCh38.p12 chr6: 167,947,879-168,208,655 KIF25, AFDN, 5 more genes
    nsv6631217copy number variation3nstd224human GRCh37 chr6: 168,344,728-168,592,134 , GRCh38.p12 chr6: 167,944,048-168,191,454 KIF25, AFDN, 5 more genes
    nsv6631216copy number variation1nstd224human GRCh37 chr6: 168,343,838-168,621,367 , GRCh38.p12 chr6: 167,943,158-168,220,687 KIF25, AFDN, 5 more genes
    nsv6631128copy number variation2nstd224human GRCh37 chr6: 168,354,052-168,597,599 , GRCh38.p12 chr6: 167,953,372-168,196,919 KIF25, AFDN, 5 more genes
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