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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5899321copy number variation1nstd209human GRCh38 chr6: 33,796,398-33,796,481 , GRCh37.p13 chr6: 33,764,175-33,764,258 LOC105375024, MLN
    nsv5464405copy number variation1nstd206human GRCh38 chr6: 33,797,524-33,802,607 , GRCh37.p13 chr6: 33,765,301-33,770,384 LOC105375024, MLN
    nsv5456413copy number variation1nstd206human GRCh38 chr6: 33,796,398-33,796,484 , GRCh37.p13 chr6: 33,764,175-33,764,261 MLN, LOC105375024
    nsv4940783copy number variation1nstd200human GRCh38 chr6: 33,797,524-33,802,607 , GRCh37.p13 chr6: 33,765,301-33,770,384 LOC105375024, MLN
    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
    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
    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
    nsv4130464copy number variation1nstd166human GRCh37.p13 chr6: 33,761,693-33,761,762 , GRCh38.p12 chr6: 33,793,916-33,793,985 LEMD2, MLN, 1 more genes
    nsv4122871copy number variation1nstd166human GRCh37.p13 chr6: 33,764,175-33,764,261 , GRCh38.p12 chr6: 33,796,398-33,796,484 MLN, LOC105375024
    nsv3967743copy number variation1nstd168human GRCh38 chr6: 33,783,342-33,799,432 , GRCh37.p13 chr6: 33,751,119-33,767,209 LEMD2, MLN, 1 more genes
    nsv3964410insertion1nstd168human GRCh38 chr6: 33,784,811-33,829,401 , GRCh37.p13 chr6: 33,752,588-33,797,178 MLN, LEMD2, 2 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
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