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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5231786copy number variation1nstd204human GRCh38.p13 chr6: 33,016,601-33,499,100 , GRCh37.p13 chr6: 32,984,378-33,466,877 COL11A2, RXRB, 39 more genes
    nsv4768386copy number variation1nstd102humanLikely pathogenic GRCh38.p12 chr6: 33,375,382-33,468,170 , NCBI36 chr6: 33,451,137-33,543,925 , GRCh37.p13 chr6: 33,343,159-33,435,947 , GRCh37.p13 chr6|NT_167249.1: 4,836,050-4,916,187 , GRCh38.p12 chr6|NT_167249.2: 4,836,753-4,916,889 KIFC1, PHF1, 6 more genes
    nsv4757608inversion1nstd199human GRCh37 chr6: 26,743,921-58,149,359 , GRCh38.p12 chr6: 26,823,536-61,119,912 , ABCF1, 1075 more genes
    nsv4756329inversion1nstd199human GRCh37 chr6: 26,745,246-58,149,317 , GRCh38.p12 chr6: 26,823,536-61,119,912 , ABCF1, 1075 more genes
    nsv4735754copy number variation1nstd199human GRCh37 chr6: 26,776,020-58,144,810 , GRCh38.p12 chr6: 26,823,536-61,119,912 , RNU6-250P, 1075 more genes
    nsv4683878copy number variation1nstd102humanUncertain significance GRCh37 chr6: 33,359,763-33,640,005 , GRCh38.p12 chr6: 33,391,986-33,672,228 ITPR3-AS1, MIR5004, 12 more genes
    nsv4675941copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 31,036,397-34,088,832 , GRCh38.p12 chr6: 31,068,620-34,121,055 AGER, AIF1, 217 more genes
    nsv4456439copy number variation1nstd102humanUncertain significance GRCh37 chr6: 33,388,971-33,428,369 , GRCh38.p12 chr6: 33,421,194-33,460,592 SYNGAP1, MIR5004, 1 more genes
    nsv4350067copy number variation1nstd102humanPathogenic GRCh37 chr6: 29,455,465-81,447,367 , GRCh38.p12 chr6: 29,487,688-80,737,650 HLA-DPB2, CIMIP3, 1001 more genes
    nsv3913920copy number variation1nstd102humanPathogenic GRCh38 chr6: 156,974-46,789,291 , NCBI36 chr6: 101,974-46,864,987 , GRCh37 chr6: 156,974-46,757,028 TRR-ACG1-2, TMEM217, 1385 more genes
    nsv3889814copy number variation1nstd102humanPathogenic GRCh37 chr6: 165,632-170,919,470 , GRCh38.p12 chr6: 165,632-170,610,382 ITPR3, HSD17B8, 2905 more genes
    nsv3887898copy number variation2nstd102humanPathogenic GRCh37 chr6: 156,975-170,919,482 , GRCh38.p12 chr6: 156,975-170,610,394 SOD1P1, HLA-DPB1, 2905 more genes
    nsv3879811copy number variation1nstd102humanPathogenic GRCh37 chr6: 108,666-170,980,171 , GRCh38.p12 chr6: 108,666-170,671,083 RNU6-411P, LOC107986611, 2910 more genes
    nsv3877040copy number variation1nstd102humanPathogenic GRCh37 chr6: 60,107-171,054,786 , GRCh38.p12 chr6: 60,107-170,745,698 LOC105378061, MIR4640, 2914 more genes
    nsv3169066inversion1nstd158human GRCh37 chr6: 5,923,377-99,717,885 , GRCh38.p12 chr6: 5,923,144-99,270,009 , ABCF1, 1877 more genes
    nsv3168939inversion1nstd158human GRCh37 chr6: 12,268,690-80,058,596 , GRCh38.p12 chr6: 12,268,457-79,348,879 , ABCF1, 1548 more genes
    nsv3168805inversion1nstd158human GRCh37 chr6: 12,296,990-80,059,394 , GRCh38.p12 chr6: 12,296,757-79,349,677 , ABCF1, 1548 more genes
    nsv3168551inversion1nstd158human GRCh37 chr6: 7,798,260-81,124,626 , GRCh38.p12 chr6: 7,798,027-80,414,909 , ABCF1, 1644 more genes
    nsv3168167copy number variation1nstd158human GRCh37 chr6: 12,299,904-158,472,787 , GRCh38.p12 chr6: 12,299,671-158,051,755 , ABCF1, 2551 more genes
    nsv3168075inversion1nstd158human GRCh37 chr6: 10,515,049-82,678,331 , GRCh38.p12 chr6: 10,514,816-81,968,614 , ABCF1, 1617 more genes
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