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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5961706insertion1nstd209human GRCh38 chr7: 77,573,104-77,573,104 , GRCh37.p13 chr7: 77,202,421-77,202,421 PTPN12
    nsv5950148insertion1nstd209human GRCh38 chr7: 77,564,746-77,564,746 , GRCh37.p13 chr7: 77,194,063-77,194,063 PTPN12
    nsv5923909copy number variation1nstd209human GRCh38 chr7: 77,638,730-77,639,216 , GRCh37.p13 chr7: 77,268,047-77,268,533 PTPN12
    nsv5913370copy number variation1nstd209human GRCh38 chr7: 77,564,979-77,565,071 , GRCh37.p13 chr7: 77,194,296-77,194,388 PTPN12
    nsv5675944mobile element insertion2nstd211human GRCh38 chr7: 77,539,152-77,539,152 , GRCh37.p13 chr7: 77,168,469-77,168,469 PTPN12
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5492180copy number variation1nstd206human GRCh38 chr7: 77,564,979-77,565,073 , GRCh37.p13 chr7: 77,194,296-77,194,390 PTPN12
    nsv5487082copy number variation1nstd206human GRCh38 chr7: 77,567,262-77,567,363 , GRCh37.p13 chr7: 77,196,579-77,196,680 PTPN12
    nsv5475226copy number variation1nstd206human GRCh38 chr7: 77,540,195-77,540,292 , GRCh37.p13 chr7: 77,169,512-77,169,609 PTPN12
    nsv5410589mobile element insertion1nstd206human GRCh38 chr7: 77,539,152-77,539,158 , GRCh37.p13 chr7: 77,168,469-77,168,475 PTPN12
    nsv5343250translocation1nstd200human GRCh37 chr7: 77,197,120-77,197,120 , GRCh37 chr7: 77,189,163-77,189,163 , GRCh38.p12 chr7: 77,559,846-77,559,846 , GRCh38.p12 chr7: 77,567,803-77,567,803 PTPN12
    nsv5334961translocation1nstd200human GRCh37 chr7: 77,268,050-77,268,050 , GRCh37 chr7: 77,268,534-77,268,534 , GRCh38.p12 chr7: 77,638,733-77,638,733 , GRCh38.p12 chr7: 77,639,217-77,639,217 PTPN12
    nsv5305700copy number variation1nstd204human GRCh38.p13 chr7: 77,539,771-77,540,338 , GRCh37.p13 chr7: 77,169,088-77,169,655 PTPN12
    nsv5304249copy number variation1nstd204human GRCh38.p13 chr7: 77,574,657-77,575,145 , GRCh37.p13 chr7: 77,203,974-77,204,462 PTPN12
    nsv5304192copy number variation1nstd204human GRCh38.p13 chr7: 77,551,539-77,551,870 , GRCh37.p13 chr7: 77,180,856-77,181,187 PTPN12
    nsv5119307mobile element insertion1nstd203human GRCh38 chr7: 77,564,746-77,564,776 , GRCh37.p13 chr7: 77,194,063-77,194,093 PTPN12
    nsv5119298mobile element insertion1nstd203human GRCh38 chr7: 77,640,429-77,640,474 , GRCh37.p13 chr7: 77,269,746-77,269,791 PTPN12
    nsv5118203mobile element insertion1nstd203human GRCh38 chr7: 77,636,024-77,636,036 , GRCh37.p13 chr7: 77,265,341-77,265,353 PTPN12
    nsv5118065mobile element insertion1nstd203human GRCh38 chr7: 77,564,744-77,564,776 , GRCh37.p13 chr7: 77,194,061-77,194,093 PTPN12
    nsv5105901mobile element insertion1nstd203human GRCh38 chr7: 77,613,159-77,613,192 , GRCh37.p13 chr7: 77,242,476-77,242,509 PTPN12
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