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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
    nsv7146925copy number variation1nstd232human GRCh37.p13 chr6: 168,402,880-168,402,947 , GRCh38.p12 chr6: 168,002,200-168,002,267 KIF25
    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
    nsv6817683copy number variation1nstd229human GRCh38 chr6: 168,013,237-168,013,756 , GRCh37.p13 chr6: 168,413,917-168,414,436 KIF25
    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
    nsv6812766copy number variation1nstd229human GRCh38 chr6: 168,045,155-168,045,650 , GRCh37.p13 chr6: 168,445,835-168,446,330 LOC105378135, KIF25
    nsv6812391copy number variation1nstd229human GRCh38 chr6: 167,991,948-168,082,862 , GRCh37.p13 chr6: 168,392,628-168,483,542 LOC105378135, KIF25, 2 more genes
    nsv6807113copy number variation1nstd229human GRCh38 chr6: 168,026,584-168,029,781 , GRCh37.p13 chr6: 168,427,264-168,430,461 KIF25
    nsv6805592copy number variation1nstd229human GRCh38 chr6: 168,013,642-168,013,740 , GRCh37.p13 chr6: 168,414,322-168,414,420 KIF25
    nsv6804700copy number variation1nstd229human GRCh38 chr6: 168,003,465-168,003,491 , GRCh37.p13 chr6: 168,404,145-168,404,171 KIF25
    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
    nsv6799962copy number variation1nstd229human GRCh38 chr6: 168,009,223-168,014,020 , GRCh37.p13 chr6: 168,409,903-168,414,700 KIF25
    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
    nsv6798692copy number variation1nstd229human GRCh38 chr6: 168,017,172-168,022,988 , GRCh37.p13 chr6: 168,417,852-168,423,668 KIF25
    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
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