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Items: 1 to 20 of 224

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7040013inversion1nstd229human GRCh38 chr3: 149,738,106-150,684,675 , GRCh37.p13 chr3: 149,455,893-150,402,462 RPL32P9, COMMD2, 25 more genes
    nsv6728853copy number variation1nstd229human GRCh38 chr3: 150,704,829-150,704,865 , GRCh37.p13 chr3: 150,422,616-150,422,652 ERICH6, ERICH6-AS1
    nsv6726618copy number variation1nstd229human GRCh38 chr3: 150,703,172-150,709,406 , GRCh37.p13 chr3: 150,420,959-150,427,193 ERICH6, ERICH6-AS1
    nsv6726084copy number variation1nstd229human GRCh38 chr3: 150,702,301-150,780,300 , GRCh37.p13 chr3: 150,420,088-150,498,087 SIAH2-AS1, ERICH6-AS1, 4 more genes
    nsv6718091copy number variation1nstd229human GRCh38 chr3: 150,664,293-150,668,170 , GRCh37.p13 chr3: 150,382,080-150,385,957 ERICH6
    nsv6637156copy number variation1nstd102humanPathogenic GRCh37 chr3: 116,620,308-172,042,292 , GRCh38.p12 chr3: 116,901,461-172,324,502 H1-10, AADACL2-AS1, 846 more genes
    nsv6574415inversion1nstd223human GRCh38 chr3: 150,678,800-150,679,852 , GRCh37.p13 chr3: 150,396,587-150,397,639 ERICH6
    nsv6556814inversion1nstd223human GRCh38 chr3: 150,675,049-150,675,472 , GRCh37.p13 chr3: 150,392,836-150,393,259 ERICH6
    nsv6365922copy number variation1nstd223human GRCh38 chr3: 150,662,918-150,664,681 , GRCh37.p13 chr3: 150,380,705-150,382,468 ERICH6
    nsv6359114copy number variation1nstd223human GRCh38 chr3: 150,689,901-150,694,200 , GRCh37.p13 chr3: 150,407,688-150,411,987 ERICH6
    nsv6313678copy number variation1nstd102humanPathogenic GRCh37 chr3: 145,486,960-160,504,834 , GRCh38.p12 chr3: 145,769,173-160,787,046 RNU6-901P, RPL32P8, 229 more genes
    nsv6311444copy number variation1nstd102humanPathogenic GRCh37 chr3: 148,447,967-151,176,497 , GRCh38.p12 chr3: 148,730,180-151,458,709 TM4SF1, FKBP1AP4, 68 more genes
    nsv6290273copy number variation1nstd102humanPathogenic GRCh37 chr3: 142,729,607-157,921,084 , GRCh38.p12 chr3: 143,010,765-158,203,295 LINC02066, TM4SF1-AS1, 206 more genes
    nsv6290244copy number variation1nstd102humanPathogenic GRCh37 chr3: 143,439,359-165,252,122 , GRCh38.p12 chr3: 143,720,517-165,534,334 LOC102724145, C3orf80, 273 more genes
    nsv5949539insertion1nstd209human GRCh38 chr3: 150,672,264-150,672,264 , GRCh37.p13 chr3: 150,390,051-150,390,051 ERICH6
    nsv5897910copy number variation1nstd209human GRCh38 chr3: 150,704,668-150,704,883 , GRCh37.p13 chr3: 150,422,455-150,422,670 ERICH6, ERICH6-AS1
    nsv5683149mobile element insertion1nstd211human GRCh38 chr3: 150,659,919-150,659,919 , GRCh37.p13 chr3: 150,377,706-150,377,706 ERICH6
    nsv5681515mobile element insertion2nstd211human GRCh38 chr3: 150,681,070-150,681,070 , GRCh37.p13 chr3: 150,398,857-150,398,857 ERICH6
    nsv5445303copy number variation1nstd206human GRCh38 chr3: 150,662,918-150,664,681 , GRCh37.p13 chr3: 150,380,705-150,382,468 ERICH6
    nsv5401524mobile element insertion1nstd206human GRCh38 chr3: 150,659,919-150,659,970 , GRCh37.p13 chr3: 150,377,706-150,377,757 ERICH6
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