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Items: 1 to 20 of 629

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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
    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
    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
    nsv6631164copy number variation1nstd224human GRCh37 chr6: 31,963,844-32,011,639 , GRCh38.p12 chr6: 31,996,067-32,043,862 C4A, C4B, 5 more genes
    nsv6631044copy number variation1nstd224human GRCh37 chr6: 31,975,129-32,013,975 , GRCh38.p12 chr6: 32,007,352-32,046,198 C4B, CYP21A2, 4 more genes
    nsv6630975copy number variation1nstd224human GRCh37 chr6: 31,963,844-32,009,407 , GRCh38.p12 chr6: 31,996,067-32,041,630 C4A, C4B, 5 more genes
    nsv6409596copy number variation1nstd223human GRCh38 chr6: 32,006,101-32,007,600 , GRCh37.p13 chr6: 31,973,878-31,975,377 CYP21A1P, TNXA
    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
    nsv6398904copy number variation1nstd223human GRCh38 chr6: 32,004,401-32,007,700 , GRCh37.p13 chr6: 31,972,178-31,975,477 CYP21A1P, TNXA
    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
    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
    nsv6064380insertion1nstd212human GRCh38 chr6: 32,010,984-32,010,984 , GRCh37.p13 chr6: 31,978,761-31,978,761 TNXA
    nsv6015913copy number variation1nstd212human GRCh38 chr6: 31,984,691-32,023,790 , GRCh37.p13 chr6: 31,952,468-31,991,567 C4A, C4B, 3 more genes
    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
    nsv6003594copy number variation1nstd212human GRCh38 chr6: 31,991,052-32,017,425 , GRCh37.p13 chr6: 31,958,829-31,985,202 C4A, C4B, 3 more genes
    nsv5904348copy number variation1nstd209human GRCh38 chr6: 32,004,720-32,037,360 , GRCh37.p13 chr6: 31,972,497-32,005,137 C4B, CYP21A2, 3 more genes
    nsv5845135copy number variation3nstd209human GRCh38 chr6: 32,004,448-32,007,470 , GRCh37.p13 chr6: 31,972,225-31,975,247 CYP21A1P, TNXA
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