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Items: 1 to 20 of 253

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5898260copy number variation1nstd209human GRCh38 chr5: 156,986,485-157,423,872 , GRCh37.p13 chr5: 156,413,496-156,850,880 ITK, MED7, 7 more genes
    nsv5684302mobile element insertion1nstd211human GRCh38 chr5: 157,312,283-157,312,283 , GRCh37.p13 chr5: 156,739,291-156,739,291 CYFIP2
    nsv5549858insertion1nstd206human GRCh38 chr5: 157,302,081-157,302,096 , GRCh37.p13 chr5: 156,729,089-156,729,104 CYFIP2
    nsv5470741copy number variation1nstd206human GRCh38 chr5: 157,274,096-157,274,710 , GRCh37.p13 chr5: 156,701,106-156,701,720 CYFIP2
    nsv5464579copy number variation1nstd206human GRCh38 chr5: 157,276,398-157,280,345 , GRCh37.p13 chr5: 156,703,408-156,707,355 CYFIP2
    nsv5455271copy number variation1nstd206human GRCh38 chr5: 157,304,441-157,304,538 , GRCh37.p13 chr5: 156,731,449-156,731,546 CYFIP2
    nsv5399858mobile element insertion1nstd206human GRCh38 chr5: 157,312,283-157,312,334 , GRCh37.p13 chr5: 156,739,291-156,739,342 CYFIP2
    nsv5161367mobile element insertion1nstd203human GRCh38 chr5: 157,277,580-157,277,596 , GRCh37.p13 chr5: 156,704,590-156,704,606 CYFIP2
    nsv5096486mobile element insertion1nstd203human GRCh38 chr5: 157,312,273-157,312,283 , GRCh37.p13 chr5: 156,739,281-156,739,291 CYFIP2
    nsv5095325mobile element insertion1nstd203human GRCh38 chr5: 157,312,274-157,312,283 , GRCh37.p13 chr5: 156,739,282-156,739,291 CYFIP2
    nsv5081943mobile element insertion1nstd203human GRCh38 chr5: 157,312,269-157,312,283 , GRCh37.p13 chr5: 156,739,277-156,739,291 CYFIP2
    nsv5036421inversion1nstd200human GRCh38 chr5: 85,193,812-162,906,830 , GRCh37.p13 chr5: 84,489,630-162,333,836 , PRR16, 1116 more genes
    nsv4885569inversion1nstd200human GRCh37 chr5: 84,489,636-162,333,841 , GRCh38.p12 chr5: 85,193,818-162,906,835 , UBE2B, 1116 more genes
    nsv4674945copy number variation1nstd102humanPathogenic GRCh37 chr5: 156,347,980-169,959,880 , GRCh38.p12 chr5: 156,920,969-170,532,876 LINC02227, LINC01932, 146 more genes
    nsv4570394mobile element insertion1nstd166human GRCh37.p13 chr5: 156,704,590-156,704,590 , GRCh38.p12 chr5: 157,277,580-157,277,580 CYFIP2
    nsv4565117mobile element insertion1nstd166human GRCh37.p13 chr5: 156,744,257-156,744,257 , GRCh38.p12 chr5: 157,317,249-157,317,249 CYFIP2
    nsv4562715mobile element insertion1nstd166human GRCh37.p13 chr5: 156,739,454-156,739,454 , GRCh38.p12 chr5: 157,312,446-157,312,446 CYFIP2
    nsv4485548mobile element insertion1nstd166human GRCh37.p13 chr5: 156,739,277-156,739,277 , GRCh38.p12 chr5: 157,312,269-157,312,269 CYFIP2
    nsv4485532mobile element insertion1nstd166human GRCh37.p13 chr5: 156,739,291-156,739,291 , GRCh38.p12 chr5: 157,312,283-157,312,283 CYFIP2
    nsv4455586copy number variation1nstd102humanPathogenic GRCh37 chr5: 156,597,181-171,166,353 , GRCh38.p12 chr5: 157,170,170-171,739,349 LOC105377677, GABRA6, 164 more genes
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