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Items: 1 to 20 of 391

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5949649insertion1nstd209human GRCh38 chr7: 115,944,013-115,944,013 , GRCh37.p13 chr7: 115,584,067-115,584,067 TFEC
    nsv5921649copy number variation1nstd209human GRCh38 chr7: 116,149,761-116,149,820 , GRCh37.p13 chr7: 115,789,815-115,789,874 TFEC
    nsv5919191copy number variation1nstd209human GRCh38 chr7: 116,024,784-116,024,859 , GRCh37.p13 chr7: 115,664,838-115,664,913 TFEC
    nsv5917267copy number variation1nstd209human GRCh38 chr7: 115,943,510-115,947,744 , GRCh37.p13 chr7: 115,583,564-115,587,798 TFEC
    nsv5912000copy number variation1nstd209human GRCh38 chr7: 116,058,447-116,058,528 , GRCh37.p13 chr7: 115,698,501-115,698,582 TFEC
    nsv5862018copy number variation1nstd209human GRCh38 chr7: 115,943,494-115,947,728 , GRCh37.p13 chr7: 115,583,548-115,587,782 TFEC
    nsv5726630mobile element insertion1nstd211human GRCh38 chr7: 116,110,408-116,110,408 , GRCh37.p13 chr7: 115,750,462-115,750,462 TFEC
    nsv5723601mobile element insertion1nstd211human GRCh38 chr7: 115,955,235-115,955,235 , GRCh37.p13 chr7: 115,595,289-115,595,289 TFEC
    nsv5693810mobile element insertion1nstd211human GRCh38 chr7: 116,085,315-116,085,315 , GRCh37.p13 chr7: 115,725,369-115,725,369 TFEC
    nsv5692562mobile element insertion1nstd211human GRCh38 chr7: 115,933,600-115,933,600 , GRCh37.p13 chr7: 115,573,654-115,573,654 TFEC
    nsv5682117mobile element insertion1nstd211human GRCh38 chr7: 116,159,689-116,159,689 , GRCh37.p13 chr7: 115,799,743-115,799,743 TFEC
    nsv5681234mobile element insertion1nstd211human GRCh38 chr7: 115,962,728-115,962,728 , GRCh37.p13 chr7: 115,602,782-115,602,782 TFEC
    nsv5579457copy number variation1nstd207human GRCh38 chr7: 116,024,784-116,024,859 , GRCh37.p13 chr7: 115,664,838-115,664,913 TFEC
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5538717insertion1nstd206human GRCh38 chr7: 116,110,293-116,110,293 , GRCh37.p13 chr7: 115,750,347-115,750,347 TFEC
    nsv5478284copy number variation1nstd206human GRCh38 chr7: 115,943,513-115,947,745 , GRCh37.p13 chr7: 115,583,567-115,587,799 TFEC
    nsv5412992mobile element insertion1nstd206human GRCh38 chr7: 115,962,728-115,962,779 , GRCh37.p13 chr7: 115,602,782-115,602,833 TFEC
    nsv5402036mobile element insertion1nstd206human GRCh38 chr7: 115,933,600-115,933,651 , GRCh37.p13 chr7: 115,573,654-115,573,705 TFEC
    nsv5398129mobile element insertion1nstd206human GRCh38 chr7: 116,159,689-116,159,740 , GRCh37.p13 chr7: 115,799,743-115,799,794 TFEC
    nsv5371045translocation1nstd200human GRCh38 chr7: 116,058,451-116,058,451 , GRCh38 chr7: 116,058,529-116,058,529 , GRCh37.p13 chr7: 115,698,583-115,698,583 , GRCh37.p13 chr7: 115,698,505-115,698,505 TFEC
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