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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5844006copy number variation1nstd209human GRCh38 chr6: 12,266,725-12,272,624 , GRCh37.p13 chr6: 12,266,958-12,272,857 EDN1
    nsv5638613insertion1nstd207human GRCh38 chr6: 12,284,672-12,284,672 , GRCh37.p13 chr6: 12,284,905-12,284,905 EDN1
    nsv5300624copy number variation1nstd204human GRCh38.p13 chr6: 12,281,379-12,283,219 , GRCh37.p13 chr6: 12,281,612-12,283,452 EDN1
    nsv4934422copy number variation1nstd200human GRCh38 chr6: 12,039,183-12,255,228 , GRCh37.p13 chr6: 12,039,416-12,255,461 HIVEP1, EDN1
    nsv4934387copy number variation1nstd200human GRCh38 chr6: 7,366,072-12,459,747 , GRCh37.p13 chr6: 7,366,305-12,459,979 , DSP, 90 more genes
    nsv4729581copy number variation1nstd102humanUncertain significance GRCh37 chr6: 11,881,588-12,570,991 , GRCh38.p12 chr6: 11,881,355-12,570,759 HIVEP1, LOC105374931, 6 more genes
    nsv4729499copy number variation1nstd102humanUncertain significance GRCh37 chr6: 12,039,246-12,255,731 , GRCh38.p12 chr6: 12,039,013-12,255,498 EDN1, HIVEP1
    nsv4675202copy number variation1nstd102humanUncertain significance GRCh37 chr6: 11,957,257-12,556,338 , GRCh38.p12 chr6: 11,957,024-12,556,106 LOC107986570, RN7SKP293, 6 more genes
    nsv4456780copy number variation1nstd102humanPathogenic GRCh37 chr6: 156,974-23,221,621 , GRCh38.p12 chr6: 156,974-23,221,393 LOC105374960, LOC101928573, 342 more genes
    nsv4324882inversion1nstd166human GRCh37.p13 chr6: 11,087,007-14,472,606 , GRCh38.p12 chr6: 11,086,774-14,472,375 , HIVEP1, 56 more genes
    nsv4130339copy number variation1nstd166human GRCh37.p13 chr6: 12,039,392-12,255,461 , GRCh38.p12 chr6: 12,039,159-12,255,228 HIVEP1, EDN1
    nsv4129499copy number variation1nstd166human GRCh37.p13 chr6: 12,262,169-12,262,250 , GRCh38.p12 chr6: 12,261,936-12,262,017 EDN1
    nsv4119003copy number variation1nstd166human GRCh37.p13 chr6: 12,272,354-12,276,152 , GRCh38.p12 chr6: 12,272,121-12,275,919 EDN1
    nsv3922052copy number variation1nstd102humanPathogenic GRCh37 chr6: 155,807-17,058,645 , NCBI36 chr6: 100,807-17,166,624 , GRCh38 chr6: 155,807-17,058,414 ECI2-DT, RNU1-11P, 268 more genes
    nsv3921817copy number variation1nstd102humanPathogenic GRCh37 chr6: 2,862,874-16,698,019 , GRCh38 chr6: 2,862,640-16,697,788 , NCBI36 chr6: 2,807,873-16,805,998 RN7SKP293, LOC105374906, 230 more genes
    nsv3921027copy number variation1nstd102humanPathogenic GRCh38 chr6: 389,423-13,474,956 , GRCh37 chr6: 389,423-13,475,188 , NCBI36 chr6: 334,423-13,583,167 LOC105374898, HIVEP1, 215 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
    nsv3918220copy number variation1nstd102humanPathogenic GRCh38 chr6: 10,601,499-13,987,316 , NCBI36 chr6: 10,709,718-14,095,526 , GRCh37 chr6: 10,601,732-13,987,547 GCNT2, LOC105374935, 58 more genes
    nsv3914672copy number variation1nstd102humanLikely pathogenic NCBI36 chr6: 101,974-13,189,419 , GRCh37 chr6: 156,974-13,081,433 , GRCh38 chr6: 156,974-13,081,201 BMP6, BPHL, 212 more genes
    nsv3914068copy number variation1nstd102humanPathogenic NCBI36 chr6: 4,014,025-13,376,010 , GRCh38 chr6: 4,068,792-13,267,799 , GRCh37 chr6: 4,069,026-13,268,031 SSR1, LOC107986560, 145 more genes
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