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Items: 1 to 20 of 152

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097426copy number variation1nstd102humanUncertain significance GRCh37 chr6: 30,695,893-36,953,949 , GRCh38.p12 chr6: 30,728,116-36,986,173 LEMD2, PSORS1C1, 321 more genes
    nsv7097325copy number variation1nstd102humanUncertain significance GRCh37 chr6: 30,695,893-31,937,492 , GRCh38.p12 chr6: 30,728,116-31,969,715 HCG21, SNORD84, 117 more genes
    nsv7053830inversion1nstd229human GRCh38 chr6: 29,164,448-38,692,657 , GRCh37.p13 chr6: 29,132,225-38,660,433 GTF2H4, RNF8, 472 more genes
    nsv7045112inversion1nstd229human GRCh38 chr6: 30,561,326-37,907,708 , GRCh37.p13 chr6: 30,529,103-37,875,484 ZBTB22, PNPLA1, 355 more genes
    nsv6787643copy number variation1nstd229human GRCh38 chr6: 31,716,642-31,762,100 , GRCh37.p13 chr6: 31,684,419-31,729,877 DDAH2, LY6G6F-LY6G6D, 9 more genes
    nsv6414744copy number variation1nstd223human GRCh38 chr6: 31,714,798-31,723,443 , GRCh37.p13 chr6: 31,682,575-31,691,220 MPIG6B, LY6G6F-LY6G6D, 2 more genes
    nsv6402266copy number variation1nstd223human GRCh38 chr6: 31,522,086-32,653,908 , GRCh37.p13 chr6: 31,489,863-32,621,685 MIR6833, LY6G5B, 102 more genes
    nsv6135917copy number variation1nstd213human GRCh37 chr6: 30,110,000-32,450,001 , GRCh38.p12 chr6: 30,142,223-32,482,224 ABCF1, AGER, 186 more genes
    nsv5234405copy number variation1nstd204human GRCh38.p13 chr6: 30,240,001-32,313,700 , GRCh37.p13 chr6: 30,207,778-32,281,477 DDAH2, LOC105375018, 175 more genes
    nsv5229879copy number variation1nstd204human GRCh38.p13 chr6: 31,502,001-32,151,900 , GRCh37.p13 chr6: 31,469,778-32,119,677 LTB, PPT2, 80 more genes
    nsv5229526copy number variation1nstd204human GRCh38.p13 chr6: 31,620,501-31,855,300 , GRCh37.p13 chr6: 31,588,278-31,823,077 LOC105375018, DDAH2, 35 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
    nsv4706993copy number variation1nstd195human GRCh37 chr6: 31,587,351-31,783,751 , GRCh38.p12 chr6: 31,619,574-31,815,974 BAG6, ABHD16A, 31 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
    nsv3921657copy number variation1nstd102humanUncertain significance NCBI36 chr6: 31,773,217-31,934,913 , GRCh37.p13 chr6|NT_167245.1: 2,950,808-3,112,520 , GRCh37.p13 chr6|NT_167247.1: 3,044,917-3,154,498 , GRCh37.p13 chr6|NT_167249.1: 3,054,967-3,159,682 , GRCh37.p13 chr6|NT_167244.1: 3,037,483-3,141,689 , GRCh37.p13 chr6: 31,665,238-31,826,934 , GRCh38.p12 chr6: 31,697,461-31,859,157 , GRCh38.p12 chr6|NT_167247.2: 3,039,332-3,148,913 , GRCh38.p12 chr6|NT_167249.2: 3,055,670-3,160,384 , GRCh38.p12 chr6|NT_167245.2: 2,945,223-3,106,935 , GRCh38.p12 chr6|NT_167244.2: 3,087,568-3,191,773 CLIC1, SAPCD1, 24 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
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