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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5114798mobile element insertion1nstd203human GRCh38 chr6: 25,852,232-25,852,248 , GRCh37.p13 chr6: 25,852,460-25,852,476 SLC17A3
    nsv4940454copy number variation1nstd200human GRCh38 chr6: 25,860,986-25,861,109 , GRCh37.p13 chr6: 25,861,214-25,861,337 SLC17A3
    nsv4940453copy number variation1nstd200human GRCh38 chr6: 25,848,375-25,853,086 , GRCh37.p13 chr6: 25,848,603-25,853,314 SLC17A3
    nsv4815669copy number variation1nstd200human GRCh37 chr6: 25,848,603-25,853,314 , GRCh38.p12 chr6: 25,848,375-25,853,086 SLC17A3
    nsv4729301copy number variation1nstd102humanUncertain significance GRCh37 chr6: 25,622,751-25,853,825 , GRCh38.p12 chr6: 25,622,523-25,853,597 H2AC1, SLC17A4, 7 more genes
    nsv4119181copy number variation1nstd166human GRCh37.p13 chr6: 25,851,483-25,852,021 , GRCh38.p12 chr6: 25,851,255-25,851,793 SLC17A3
    nsv4113242copy number variation1nstd166human GRCh37.p13 chr6: 25,838,585-25,851,200 , GRCh38.p12 chr6: 25,838,357-25,850,972 SLC17A3
    nsv3922819copy number variation1nstd102humanUncertain significance NCBI36 chr6: 23,360,729-26,075,484 , GRCh37 chr6: 23,252,750-25,967,505 , GRCh38 chr6: 23,252,522-25,967,277 KAAG1, ACOT13, 52 more genes
    nsv3920564copy number variation1nstd102humanPathogenic GRCh38 chr6: 3,224,310-30,657,190 , GRCh37 chr6: 3,224,544-30,624,967 , NCBI36 chr6: 3,169,543-30,732,946 PRELID1P2, RPL7AP7, 785 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
    nsv3888702copy number variation1nstd102humanUncertain significance GRCh37 chr6: 25,851,789-26,319,486 , GRCh38.p12 chr6: 25,851,561-26,319,258 TRIM38, TRR-TCG4-1, 54 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
    nsv3872128copy number variation1nstd102humanUncertain significance GRCh37 chr6: 25,839,165-26,536,884 , GRCh38.p12 chr6: 25,838,937-26,536,656 HFE-AS1, H2AC7, 78 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
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