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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5934693copy number variation1nstd209human GRCh38 chr12: 52,047,883-52,048,322 , GRCh37.p13 chr12: 52,441,667-52,442,106 LOC107984510, NR4A1
    nsv5510197copy number variation1nstd206human GRCh38 chr12: 52,048,317-52,049,569 , GRCh37.p13 chr12: 52,442,101-52,443,353 NR4A1, LOC107984510
    nsv5509577copy number variation1nstd206human GRCh38 chr12: 52,030,660-52,032,095 , GRCh37.p13 chr12: 52,424,444-52,425,879 NR4A1
    nsv5504920copy number variation1nstd206human GRCh38 chr12: 52,029,391-52,032,110 , GRCh37.p13 chr12: 52,423,175-52,425,894 NR4A1
    nsv5501538copy number variation1nstd206human GRCh38 chr12: 52,047,877-52,048,323 , GRCh37.p13 chr12: 52,441,661-52,442,107 NR4A1, LOC107984510
    nsv5384916mobile element deletion1nstd186human GRCh37 chr12: 52,441,656-52,441,963 , GRCh38.p12 chr12: 52,047,872-52,048,179 LOC107984510, NR4A1
    nsv5384313mobile element deletion1nstd186human GRCh37 chr12: 52,441,662-52,441,963 , GRCh38.p12 chr12: 52,047,878-52,048,179 LOC107984510, NR4A1
    nsv5312137copy number variation1nstd204human GRCh38.p13 chr12: 52,047,819-52,048,510 , GRCh37.p13 chr12: 52,441,603-52,442,294 NR4A1, LOC107984510
    nsv5305722copy number variation1nstd204human GRCh38.p13 chr12: 52,047,309-52,050,867 , GRCh37.p13 chr12: 52,441,093-52,444,651 NR4A1, LOC107984510
    nsv5278272copy number variation1nstd204human GRCh38.p13 chr12: 52,048,001-52,048,400 , GRCh37.p13 chr12: 52,441,785-52,442,184 LOC107984510, NR4A1
    nsv5263148copy number variation1nstd204human GRCh38.p13 chr12: 52,047,319-52,050,868 , GRCh37.p13 chr12: 52,441,103-52,444,652 LOC107984510, NR4A1
    nsv5138185mobile element insertion1nstd203human GRCh38 chr12: 52,049,658-52,049,669 , GRCh37.p13 chr12: 52,443,442-52,443,453 NR4A1, LOC107984510
    nsv5040224inversion1nstd200human GRCh38 chr12: 47,213,128-71,357,206 , GRCh37.p13 chr12: 47,606,911-71,750,986 NR4A1, PPIAP45, 686 more genes
    nsv4972695copy number variation1nstd200human GRCh38 chr12: 52,025,797-52,026,865 , GRCh37.p13 chr12: 52,419,581-52,420,649 NR4A1
    nsv4899780mobile element deletion1nstd200human GRCh38 chr12: 52,047,878-52,048,179 , GRCh37.p13 chr12: 52,441,662-52,441,963 LOC107984510, NR4A1
    nsv4845639copy number variation1nstd200human GRCh37 chr12: 52,419,581-52,420,649 , GRCh38.p12 chr12: 52,025,797-52,026,865 NR4A1
    nsv4842734copy number variation1nstd200human GRCh37 chr12: 52,441,097-52,444,650 , GRCh38.p12 chr12: 52,047,313-52,050,866 LOC107984510, NR4A1
    nsv4775083mobile element deletion1nstd200human GRCh37 chr12: 52,441,589-52,442,209 , GRCh38.p12 chr12: 52,047,805-52,048,425 LOC107984510, NR4A1
    nsv4755205inversion1nstd199human GRCh37 chr12: 25,956,127-125,801,151 , GRCh38.p12 chr12: 25,803,193-125,316,605 ACACB, ACADS, 1787 more genes
    nsv4736781copy number variation1nstd199human GRCh37 chr12: 25,957,322-125,801,148 , GRCh38.p12 chr12: 25,804,388-125,316,602 RNA5SP368, LINC02555, 1787 more genes
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