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Items: 1 to 20 of 272

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5888323copy number variation1nstd209human GRCh38 chr4: 55,964,770-55,966,231 , GRCh37.p13 chr4: 56,830,936-56,832,397 CEP135
    nsv5727519mobile element insertion2nstd211human GRCh38 chr4: 55,956,543-55,956,543 , GRCh37.p13 chr4: 56,822,709-56,822,709 CEP135
    nsv5687794mobile element insertion1nstd211human GRCh38 chr4: 56,030,272-56,030,272 , GRCh37.p13 chr4: 56,896,438-56,896,438 CEP135
    nsv5676308mobile element insertion2nstd211human GRCh38 chr4: 55,971,638-55,971,638 , GRCh37.p13 chr4: 56,837,804-56,837,804 CEP135
    nsv5674237copy number variation1nstd102humanPathogenic GRCh38 chr4: 51,891,814-76,009,719 , GRCh37.p13 chr4: 52,757,980-76,930,872 FTLP10, RNU6-410P, 335 more genes
    nsv5470117copy number variation1nstd206human GRCh38 chr4: 55,960,977-55,961,725 , GRCh37.p13 chr4: 56,827,143-56,827,891 CEP135
    nsv5413797mobile element insertion1nstd206human GRCh38 chr4: 56,030,272-56,030,323 , GRCh37.p13 chr4: 56,896,438-56,896,489 CEP135
    nsv5399531mobile element insertion1nstd206human GRCh38 chr4: 55,971,638-55,971,689 , GRCh37.p13 chr4: 56,837,804-56,837,855 CEP135
    nsv5341480translocation1nstd200human GRCh37 chr4: 56,830,936-56,830,936 , GRCh37 chr4: 56,832,398-56,832,398 , GRCh38.p12 chr4: 55,964,770-55,964,770 , GRCh38.p12 chr4: 55,966,232-55,966,232 CEP135
    nsv5339122translocation1nstd200human GRCh37 chr4: 56,832,355-56,832,355 , GRCh37 chr4: 56,830,625-56,830,625 , GRCh38.p12 chr4: 55,964,459-55,964,459 , GRCh38.p12 chr4: 55,966,189-55,966,189 CEP135
    nsv5232238copy number variation1nstd204human GRCh38.p13 chr4: 55,994,866-55,995,915 , GRCh37.p13 chr4: 56,861,032-56,862,081 CEP135
    nsv5097981mobile element insertion1nstd203human GRCh38 chr4: 55,971,626-55,971,638 , GRCh37.p13 chr4: 56,837,792-56,837,804 CEP135
    nsv5093593mobile element insertion1nstd203human GRCh38 chr4: 55,958,468-55,958,478 , GRCh37.p13 chr4: 56,824,634-56,824,644 CEP135
    nsv5085761mobile element insertion1nstd203human GRCh38 chr4: 56,010,730-56,010,746 , GRCh37.p13 chr4: 56,876,896-56,876,912 CEP135
    nsv5039232inversion1nstd200human GRCh38 chr4: 9,660,225-57,055,279 , GRCh37.p13 chr4: 9,661,849-57,921,445 , KRT18P63, 533 more genes
    nsv5034204inversion1nstd200human GRCh38 chr4: 45,103,677-117,623,076 , GRCh37.p13 chr4: 45,105,694-118,544,231 , LOC100129728, 913 more genes
    nsv4913389copy number variation1nstd200human GRCh38 chr4: 56,024,875-56,032,304 , GRCh37.p13 chr4: 56,891,041-56,898,470 CEP135
    nsv4878267inversion1nstd200human GRCh37 chr4: 45,105,694-118,544,231 , GRCh38.p12 chr4: 45,103,677-117,623,076 , MIR367, 913 more genes
    nsv4761770inversion1nstd199human GRCh37 chr4: 34,988-191,015,248 , GRCh38.p12 chr4: 34,988-190,094,093 , ADD1, 2433 more genes
    nsv4758212inversion1nstd199human GRCh37 chr4: 30,775-191,019,445 , GRCh38.p12 chr4: 30,775-190,098,290 , ADD1, 2433 more genes
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