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Items: 1 to 20 of 307

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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
    nsv6792072copy number variation1nstd229human GRCh38 chr6: 31,977,409-31,978,008 , GRCh37.p13 chr6: 31,945,186-31,945,785 STK19
    nsv6780764copy number variation1nstd229human GRCh38 chr6: 31,969,696-31,976,304 , GRCh37.p13 chr6: 31,937,473-31,944,081 SKIC2, DXO, 1 more genes
    nsv6779807copy number variation1nstd229human GRCh38 chr6: 31,800,134-32,311,768 , GRCh37.p13 chr6: 31,767,911-32,279,545 NELFE, CYP21A1P, 43 more genes
    nsv6415414copy number variation1nstd223human GRCh38 chr6: 31,977,606-31,977,744 , GRCh37.p13 chr6: 31,945,383-31,945,521 STK19
    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
    nsv6303216copy number variation1nstd186human GRCh37 chr6: 31,945,120-31,945,715 , GRCh38.p12 chr6: 31,977,343-31,977,938 STK19
    nsv6300907copy number variation1nstd186human GRCh37 chr6: 31,948,877-32,013,777 , GRCh38.p12 chr6: 31,981,100-32,046,000 C4A, C4B, 6 more genes
    nsv6178838copy number variation1nstd214human GRCh38 chr6: 31,975,815-31,975,941 , GRCh37.p13 chr6: 31,943,592-31,943,718 STK19
    nsv6140684copy number variation1nstd206human GRCh38 chr6: 31,981,100-32,046,000 , GRCh37.p13 chr6: 31,948,877-32,013,777 C4A, C4B, 6 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
    nsv6117673copy number variation1nstd186human GRCh37 chr6: 31,948,777-32,013,177 , GRCh38.p12 chr6: 31,981,000-32,045,400 C4A, C4B, 6 more genes
    nsv6013886copy number variation1nstd212human GRCh38 chr6: 31,979,193-31,979,248 , GRCh37.p13 chr6: 31,946,970-31,947,025 STK19
    nsv6011365copy number variation1nstd212human GRCh38 chr6: 31,977,329-31,977,944 , GRCh37.p13 chr6: 31,945,106-31,945,721 STK19
    nsv6007166copy number variation1nstd212human GRCh38 chr6: 31,980,532-32,046,126 , GRCh37.p13 chr6: 31,948,309-32,013,903 C4A, C4B, 6 more genes
    nsv5898146copy number variation1nstd209human GRCh38 chr6: 31,977,322-31,977,937 , GRCh37.p13 chr6: 31,945,099-31,945,714 STK19
    nsv5466552copy number variation1nstd206human GRCh38 chr6: 31,977,343-31,977,938 , GRCh37.p13 chr6: 31,945,120-31,945,715 STK19
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