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Items: 1 to 20 of 586

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5898876copy number variation1nstd209human GRCh38 chr4: 169,441,695-169,445,194 , GRCh37.p13 chr4: 170,362,846-170,366,345 NEK1
    nsv5897151copy number variation1nstd209human GRCh38 chr4: 169,425,106-169,425,197 , GRCh37.p13 chr4: 170,346,257-170,346,348 NEK1
    nsv5838684copy number variation1nstd209human GRCh38 chr4: 169,441,643-169,445,195 , GRCh37.p13 chr4: 170,362,794-170,366,346 NEK1
    nsv5723981mobile element insertion1nstd211human GRCh38 chr4: 169,522,349-169,522,349 , GRCh37.p13 chr4: 170,443,500-170,443,500 NEK1
    nsv5721716mobile element insertion1nstd211human GRCh38 chr4: 169,522,361-169,522,361 , GRCh37.p13 chr4: 170,443,512-170,443,512 NEK1
    nsv5692675mobile element insertion1nstd211human GRCh38 chr4: 169,544,068-169,544,068 , GRCh37.p13 chr4: 170,465,219-170,465,219 NEK1
    nsv5685104mobile element insertion2nstd211human GRCh38 chr4: 169,495,199-169,495,199 , GRCh37.p13 chr4: 170,416,350-170,416,350 NEK1
    nsv5684500mobile element insertion1nstd211human GRCh38 chr4: 169,502,750-169,502,750 , GRCh37.p13 chr4: 170,423,901-170,423,901 NEK1
    nsv5682289mobile element insertion2nstd211human GRCh38 chr4: 169,425,913-169,425,913 , GRCh37.p13 chr4: 170,347,064-170,347,064 NEK1
    nsv5632154insertion1nstd207human GRCh38 chr4: 169,445,865-169,445,865 , GRCh37.p13 chr4: 170,367,016-170,367,016 NEK1
    nsv5627441insertion1nstd207human GRCh38 chr4: 169,495,188-169,495,188 , GRCh37.p13 chr4: 170,416,339-170,416,339 NEK1
    nsv5581383copy number variation1nstd207human GRCh38 chr4: 169,495,227-169,495,540 , GRCh37.p13 chr4: 170,416,378-170,416,691 NEK1
    nsv5564649copy number variation1nstd207human GRCh38 chr4: 169,467,689-169,467,836 , GRCh37.p13 chr4: 170,388,840-170,388,987 NEK1
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    nsv5465064copy number variation1nstd206human GRCh38 chr4: 169,441,695-169,445,195 , GRCh37.p13 chr4: 170,362,846-170,366,346 NEK1
    nsv5458529copy number variation1nstd206human GRCh38 chr4: 169,530,821-169,533,747 , GRCh37.p13 chr4: 170,451,972-170,454,898 NEK1
    nsv5456269copy number variation1nstd206human GRCh38 chr4: 169,419,570-169,424,415 , GRCh37.p13 chr4: 170,340,721-170,345,566 NEK1
    nsv5410967mobile element insertion1nstd206human GRCh38 chr4: 169,495,199-169,495,250 , GRCh37.p13 chr4: 170,416,350-170,416,401 NEK1
    nsv5408698mobile element insertion1nstd206human GRCh38 chr4: 169,425,913-169,425,962 , GRCh37.p13 chr4: 170,347,064-170,347,113 NEK1
    nsv5402519mobile element insertion1nstd206human GRCh38 chr4: 169,495,199-169,495,205 , GRCh37.p13 chr4: 170,416,350-170,416,356 NEK1
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