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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5889961copy number variation1nstd209human GRCh38 chr6: 43,044,314-43,044,488 , GRCh37.p13 chr6: 43,012,052-43,012,226 CUL7
    nsv5726005mobile element insertion1nstd211human GRCh38 chr6: 43,050,522-43,050,522 , GRCh37.p13 chr6: 43,018,260-43,018,260 CUL7
    nsv5673766copy number variation1nstd102humanPathogenic GRCh37 chr6: 42,928,506-43,737,486 , GRCh38.p12 chr6: 42,960,768-43,769,749 SRF, POLR1C, 39 more genes
    nsv5558551sequence alteration1nstd206human GRCh38 chr6: 40,895,286-71,029,944 , GRCh37.p13 chr6: 40,863,025-71,739,647 , ACTG1P9, 405 more genes
    nsv5224950copy number variation1nstd204human GRCh38.p13 chr6: 42,543,301-43,041,600 , GRCh37.p13 chr6: 42,511,039-43,009,338 , RPL7L1, 20 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
    nsv4592683copy number variation1nstd183human GRCh37 chr6: 42,627,455-43,357,404 , GRCh38.p12 chr6: 42,659,717-43,389,666 , PEX6, 36 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
    nsv4341639sequence alteration1nstd166human GRCh37.p13 chr6: 43,007,635-43,008,242 , GRCh38.p12 chr6: 43,039,897-43,040,504 CUL7
    nsv4132546copy number variation1nstd166human GRCh37.p13 chr6: 43,009,048-43,009,768 , GRCh38.p12 chr6: 43,041,310-43,042,030 CUL7
    nsv3924318copy number variation1nstd102humanPathogenic GRCh37 chr6: 42,336,296-44,558,281 , NCBI36 chr6: 42,444,274-44,666,259 , GRCh38 chr6: 42,368,558-44,590,544 MIR4642, SRF, 82 more genes
    nsv3919521copy number variation1nstd102humanPathogenic NCBI36 chr6: 37,853,123-45,729,558 , GRCh37 chr6: 37,745,145-45,621,580 , GRCh38 chr6: 37,777,369-45,653,843 RPL23P6, LOC102723789, 184 more genes
    nsv3919402copy number variation1nstd102humanPathogenic NCBI36 chr6: 42,769,519-46,417,784 , GRCh37.p13 chr6: 42,661,541-46,309,825 , GRCh38.p12 chr6: 42,693,803-46,342,088 LOC101929770, MRPS18A, 94 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
    nsv3912856copy number variation1nstd102humanPathogenic NCBI36 chr6: 41,713,777-46,588,645 , GRCh38 chr6: 41,638,061-46,512,949 , GRCh37 chr6: 41,605,799-46,480,686 PTCRA, LOC101929770, 121 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
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