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Items: 1 to 20 of 206

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6124998copy number variation1nstd186human GRCh37 chr19: 42,522,442-42,522,823 , GRCh38.p12 chr19: 42,018,290-42,018,671 GRIK5
    nsv5931106copy number variation1nstd209human GRCh38 chr19: 42,018,310-42,018,672 , GRCh37.p13 chr19: 42,522,462-42,522,824 GRIK5
    nsv5598312copy number variation1nstd207human GRCh38 chr19: 42,018,290-42,018,668 , GRCh37.p13 chr19: 42,522,442-42,522,820 GRIK5
    nsv5564519copy number variation1nstd102humanPathogenic GRCh38 chr19: 41,987,984-42,252,574 , GRCh37.p13 chr19: 42,514,712-42,756,726 GRIK5, DEDD2, 8 more genes
    nsv5564317copy number variation1nstd102humanPathogenic GRCh38 chr19: 41,983,952-42,247,520 , GRCh37.p13 chr19: 42,514,712-42,751,672 GSK3A, ZNF574, 8 more genes
    nsv5564233copy number variation1nstd102humanPathogenic GRCh38 chr19: 42,032,860-42,297,536 , GRCh37.p13 chr19: 42,537,012-42,801,688 POU2F2, ERF, 9 more genes
    nsv5564232copy number variation1nstd102humanPathogenic GRCh38 chr19: 41,952,441-42,266,625 , GRCh37.p13 chr19: 42,514,712-42,770,777 CIC, ERF, 10 more genes
    nsv5562413sequence alteration1nstd206human GRCh38 chr19: 41,797,706-42,527,281 , GRCh37.p13 chr19: 42,514,712-43,031,433 MEGF8, LIPE, 34 more genes
    nsv5554149sequence alteration1nstd206human GRCh38 chr19: 41,749,279-42,444,786 , GRCh37.p13 chr19: 42,514,712-42,948,938 ERF, CEACAM6, 32 more genes
    nsv5531886copy number variation1nstd206human GRCh38 chr19: 42,017,867-42,018,672 , GRCh37.p13 chr19: 42,522,019-42,522,824 GRIK5
    nsv5524986copy number variation1nstd206human GRCh38 chr19: 42,043,617-42,050,096 , GRCh37.p13 chr19: 42,547,769-42,554,248 GRIK5
    nsv5518849copy number variation1nstd206human GRCh38 chr19: 42,048,477-42,050,610 , GRCh37.p13 chr19: 42,552,629-42,554,762 GRIK5
    nsv5515054copy number variation1nstd206human GRCh38 chr19: 42,013,875-42,014,238 , GRCh37.p13 chr19: 42,518,027-42,518,390 GRIK5
    nsv5514985copy number variation1nstd206human GRCh38 chr19: 42,018,290-42,018,671 , GRCh37.p13 chr19: 42,522,442-42,522,823 GRIK5
    nsv5375444translocation1nstd200human GRCh38 chr19: 42,050,096-42,050,096 , GRCh38 chr19: 42,043,617-42,043,617 , GRCh37.p13 chr19: 42,554,248-42,554,248 , GRCh37.p13 chr19: 42,547,769-42,547,769 GRIK5
    nsv5325798copy number variation1nstd204human GRCh38.p13 chr19: 42,043,607-42,050,105 , GRCh37.p13 chr19: 42,547,759-42,554,257 GRIK5
    nsv5296596copy number variation1nstd204human GRCh38.p13 chr19: 42,043,874-42,051,178 , GRCh37.p13 chr19: 42,548,026-42,555,330 GRIK5
    nsv5024663copy number variation1nstd200human GRCh38 chr19: 42,006,967-42,007,269 , GRCh37.p13 chr19|NW_004775434.1: 576,006-576,308 , GRCh37.p13 chr19: 42,511,119-42,511,421 GRIK5
    nsv5020515copy number variation1nstd200human GRCh38 chr19: 42,031,979-42,034,080 , GRCh37.p13 chr19: 42,536,131-42,538,232 GRIK5
    nsv5020514copy number variation1nstd200human GRCh38 chr19: 42,023,838-42,026,537 , GRCh37.p13 chr19: 42,527,990-42,530,689 GRIK5
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