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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6784626copy number variation1nstd229human GRCh38 chr6: 47,310,968-47,369,410 , GRCh37.p13 chr6: 47,278,704-47,337,146 B3GNTL1P2
    nsv6411763copy number variation1nstd223human GRCh38 chr6: 46,841,055-48,021,507 , GRCh37.p13 chr6: 46,808,792-47,989,243 RPL27AP7, LOC105375082, 18 more genes
    nsv6396902copy number variation1nstd223human GRCh38 chr6: 47,344,273-47,390,418 , GRCh37.p13 chr6: 47,312,009-47,358,154 B3GNTL1P2, LOC105375082
    nsv6314749copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 43,636,308-64,947,206 , GRCh38.p12 chr6: 43,668,571-64,237,313 ACTG1P9, CRISP1, 245 more genes
    nsv6135921copy number variation1nstd213human GRCh37 chr6: 34,700,000-52,650,001 , GRCh38.p12 chr6: 34,732,223-52,785,203 ACTG1P9, CRISP1, 361 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
    nsv4934707copy number variation1nstd200human GRCh38 chr6: 47,365,876-47,487,591 , GRCh37.p13 chr6: 47,333,612-47,455,327 B3GNTL1P2, CD2AP, 1 more genes
    nsv4828690copy number variation1nstd200human GRCh37 chr6: 47,333,612-47,455,327 , GRCh38.p12 chr6: 47,365,876-47,487,591 CD2AP, LOC105375082, 1 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
    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
    nsv3923721copy number variation1nstd102humanPathogenic GRCh38 chr6: 45,681,671-54,212,044 , GRCh37 chr6: 45,649,408-54,076,842 , NCBI36 chr6: 45,757,386-54,184,801 PAQR8, GSTA6P, 131 more genes
    nsv3920148copy number variation1nstd102humanUncertain significance NCBI36 chr6: 47,439,977-47,807,367 , GRCh37.p13 chr6: 47,332,018-47,699,408 , GRCh38.p12 chr6: 47,364,282-47,731,672 ADGRF2, CD2AP, 6 more genes
    nsv3919465copy number variation1nstd102humanLikely pathogenic NCBI36 chr6: 45,061,475-48,062,533 , GRCh37 chr6: 44,953,497-47,954,574 , GRCh38 chr6: 44,985,760-47,986,838 ACTG1P9, RUNX2, 40 more genes
    nsv3913758copy number variation1nstd102humanLikely pathogenic NCBI36 chr6: 47,267,474-51,400,063 , GRCh37 chr6: 47,159,515-51,292,104 , GRCh38 chr6: 47,191,779-51,427,306 CRISP1, FTH1P5, 46 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
    nsv3884243copy number variation1nstd102humanPathogenic GRCh37 chr6: 43,636,308-50,947,320 , GRCh38.p12 chr6: 43,668,571-50,979,607 GLYATL3, RNU6-754P, 105 more genes
    nsv3881451copy number variation1nstd102humanLikely benign GRCh37 chr6: 46,984,994-47,569,904 , GRCh38.p12 chr6: 47,017,258-47,602,168 LOC105375082, B3GNTL1P2, 6 more genes
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