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Items: 1 to 20 of 242

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7141855insertion1nstd232human GRCh37.p13 chr1: 110,129,506-110,129,506 , GRCh38.p12 chr1: 109,586,884-109,586,884 GNAI3
    nsv7138808copy number variation1nstd232human GRCh37.p13 chr1: 110,134,875-110,134,963 , GRCh38.p12 chr1: 109,592,253-109,592,341 GNAI3
    nsv7099223copy number variation1nstd231human GRCh38.p12 chr1: 108,551,579-110,710,631 , GRCh37 chr1: 109,094,201-111,253,253 ALX3, AMPD2, 74 more genes
    nsv7095739copy number variation1nstd102humanPathogenic GRCh37 chr1: 108,679,275-111,674,176 , GRCh38.p12 chr1: 108,136,653-111,131,554 RPL7L1P21, GSTM4, 90 more genes
    nsv6639757copy number variation1nstd229human GRCh38 chr1: 109,586,884-109,592,042 , GRCh37.p13 chr1: 110,129,506-110,134,664 RNU6V, GNAI3
    nsv6639670copy number variation1nstd229human GRCh38 chr1: 109,570,213-109,574,936 , GRCh37.p13 chr1: 110,112,835-110,117,558 GNAI3
    nsv6639343copy number variation1nstd229human GRCh38 chr1: 109,550,414-109,550,456 , GRCh37.p13 chr1: 110,093,036-110,093,078 GNAI3
    nsv6546407inversion1nstd223human GRCh38 chr1: 109,577,531-109,578,350 , GRCh37.p13 chr1: 110,120,153-110,120,972 GNAI3
    nsv6544021inversion1nstd223human GRCh38 chr1: 109,577,279-109,578,343 , GRCh37.p13 chr1: 110,119,901-110,120,965 GNAI3
    nsv6334774copy number variation1nstd223human GRCh38 chr1: 109,574,341-109,575,193 , GRCh37.p13 chr1: 110,116,963-110,117,815 GNAI3
    nsv6332016copy number variation1nstd223human GRCh38 chr1: 109,570,676-109,571,365 , GRCh37.p13 chr1: 110,113,298-110,113,987 GNAI3
    nsv6317266copy number variation1nstd223human GRCh38 chr1: 109,583,513-109,583,843 , GRCh37.p13 chr1: 110,126,135-110,126,465 GNAI3
    nsv6316449copy number variation1nstd223human GRCh38 chr1: 109,571,897-109,573,694 , GRCh37.p13 chr1: 110,114,519-110,116,316 GNAI3
    nsv6313675copy number variation1nstd102humanPathogenic GRCh37 chr1: 95,046,805-114,714,931 , GRCh38.p12 chr1: 94,581,249-114,172,309 LINC01307, FTLP17, 320 more genes
    nsv6290678copy number variation1nstd102humanUncertain significance GRCh37 chr1: 108,346,477-110,177,123 , GRCh38.p12 chr1: 107,803,855-109,634,501 SYPL2, NDUFB3P1, 53 more genes
    nsv6133726copy number variation1nstd213human GRCh37 chr1: 109,950,000-110,240,001 , GRCh38.p12 chr1: 109,407,378-109,697,379 AMPD2, GNAI3, 14 more genes
    nsv5883412copy number variation1nstd209human GRCh38 chr1: 109,570,515-109,571,982 , GRCh37.p13 chr1: 110,113,137-110,114,604 GNAI3
    nsv5827597copy number variation1nstd209human GRCh38 chr1: 109,570,600-109,571,999 , GRCh37.p13 chr1: 110,113,222-110,114,621 GNAI3
    nsv5431073copy number variation1nstd206human GRCh38 chr1: 109,590,493-109,903,664 , GRCh37.p13 chr1: 110,133,115-110,446,286 GSTM3, GSTM1, 12 more genes
    nsv5381058copy number variation1nstd102humanPathogenic GRCh37 chr1: 102,021,465-119,737,478 , GRCh38.p12 chr1: 101,555,909-119,194,855 AMYP1, MIR4256, 320 more genes
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