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Items: 1 to 20 of 276

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5965433insertion1nstd209human GRCh38 chr4: 102,609,158-102,609,158 , GRCh37.p13 chr4: 103,530,315-103,530,315 NFKB1, LOC105377347
    nsv5726122mobile element insertion1nstd211human GRCh38 chr4: 102,589,540-102,589,540 , GRCh37.p13 chr4: 103,510,697-103,510,697 NFKB1
    nsv5725086mobile element insertion2nstd211human GRCh38 chr4: 102,518,704-102,518,704 , GRCh37.p13 chr4: 103,439,861-103,439,861 NFKB1
    nsv5683974mobile element insertion1nstd211human GRCh38 chr4: 102,598,787-102,598,787 , GRCh37.p13 chr4: 103,519,944-103,519,944 LOC105377347, NFKB1
    nsv5683230mobile element insertion1nstd211human GRCh38 chr4: 102,569,823-102,569,823 , GRCh37.p13 chr4: 103,490,980-103,490,980 NFKB1
    nsv5673737copy number variation1nstd102humanPathogenic GRCh37 chr4: 103,488,144-103,505,977 , GRCh38.p12 chr4: 102,566,987-102,584,820 NFKB1
    nsv5609677insertion1nstd207human GRCh38 chr4: 102,598,772-102,598,772 , GRCh37.p13 chr4: 103,519,929-103,519,929 LOC105377347, NFKB1
    nsv5608597insertion1nstd207human GRCh38 chr4: 102,518,690-102,518,690 , GRCh37.p13 chr4: 103,439,847-103,439,847 NFKB1
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    nsv5556872mobile element insertion1nstd206human GRCh38 chr4: 102,518,704-102,518,755 , GRCh37.p13 chr4: 103,439,861-103,439,912 NFKB1
    nsv5547030insertion1nstd206human GRCh38 chr4: 68,996,170-113,894,177 , GRCh37.p13 chr4: 69,861,888-114,815,333 , MIR548AH, 616 more genes
    nsv5461492copy number variation1nstd206human GRCh38 chr4: 102,579,188-102,579,348 , GRCh37.p13 chr4: 103,500,345-103,500,505 NFKB1
    nsv5396357mobile element insertion1nstd206human GRCh38 chr4: 102,598,787-102,598,838 , GRCh37.p13 chr4: 103,519,944-103,519,995 LOC105377347, NFKB1
    nsv5395570mobile element insertion1nstd206human GRCh38 chr4: 102,569,823-102,569,874 , GRCh37.p13 chr4: 103,490,980-103,491,031 NFKB1
    nsv5367711translocation1nstd200human GRCh38 chr4: 102,561,282-102,561,282 , GRCh38 chr10: 6,816,574-6,816,574 , GRCh37.p13 chr10: 6,858,536-6,858,536 , GRCh37.p13 chr4: 103,482,439-103,482,439 NFKB1, LINC00707
    nsv5098843mobile element insertion1nstd203human GRCh38 chr4: 102,599,218-102,599,218 , GRCh37.p13 chr4: 103,520,375-103,520,375 NFKB1, LOC105377347
    nsv5085577mobile element insertion1nstd203human GRCh38 chr4: 102,599,545-102,599,545 , GRCh37.p13 chr4: 103,520,702-103,520,702 NFKB1, LOC105377347
    nsv5034204inversion1nstd200human GRCh38 chr4: 45,103,677-117,623,076 , GRCh37.p13 chr4: 45,105,694-118,544,231 , LOC100129728, 913 more genes
    nsv4934988copy number variation1nstd200human GRCh38 chr4: 102,579,188-102,579,348 , GRCh37.p13 chr4: 103,500,345-103,500,505 NFKB1
    nsv4878267inversion1nstd200human GRCh37 chr4: 45,105,694-118,544,231 , GRCh38.p12 chr4: 45,103,677-117,623,076 , MIR367, 913 more genes
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