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Items: 1 to 20 of 146

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5681606mobile element insertion2nstd211human GRCh38 chr7: 92,576,393-92,576,393 , GRCh37.p13 chr7: 92,205,707-92,205,707 FAM133B
    nsv5674512mobile element insertion1nstd211human GRCh38 chr7: 92,584,530-92,584,530 , GRCh37.p13 chr7: 92,213,844-92,213,844 FAM133B
    nsv5633171insertion1nstd207human GRCh38 chr7: 92,576,378-92,576,378 , GRCh37.p13 chr7: 92,205,692-92,205,692 FAM133B
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5401671mobile element insertion1nstd206human GRCh38 chr7: 92,584,530-92,584,573 , GRCh37.p13 chr7: 92,213,844-92,213,887 FAM133B
    nsv5381780copy number variation1nstd102humanPathogenic GRCh37 chr7: 87,477,185-100,333,327 , GRCh38.p12 chr7: 87,847,870-100,735,704 ARPC1A, LOC112267858, 265 more genes
    nsv5370785translocation1nstd200human GRCh38 chr7: 92,559,275-92,559,275 , GRCh38 chr7: 92,559,208-92,559,208 , GRCh37.p13 chr7: 92,188,522-92,188,522 , GRCh37.p13 chr7: 92,188,589-92,188,589 FAM133B
    nsv5335934translocation1nstd200human GRCh37 chr7: 92,188,522-92,188,522 , GRCh37 chr7: 92,188,589-92,188,589 , GRCh38.p12 chr7: 92,559,208-92,559,208 , GRCh38.p12 chr7: 92,559,275-92,559,275 FAM133B
    nsv5116940mobile element insertion1nstd203human GRCh38 chr7: 92,559,420-92,559,435 , GRCh37.p13 chr7: 92,188,734-92,188,749 FAM133B
    nsv5115061mobile element insertion1nstd203human GRCh38 chr7: 92,576,305-92,576,319 , GRCh37.p13 chr7: 92,205,619-92,205,633 FAM133B
    nsv5110335mobile element insertion1nstd203human GRCh38 chr7: 92,572,293-92,572,308 , GRCh37.p13 chr7: 92,201,607-92,201,622 FAM133B
    nsv5109433mobile element insertion1nstd203human GRCh38 chr7: 92,576,378-92,576,393 , GRCh37.p13 chr7: 92,205,692-92,205,707 FAM133B
    nsv5109069mobile element insertion1nstd203human GRCh38 chr7: 92,576,385-92,576,393 , GRCh37.p13 chr7: 92,205,699-92,205,707 FAM133B
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv5029742inversion1nstd200human GRCh38 chr7: 79,688,546-147,673,588 , GRCh37.p13 chr7: 79,317,862-147,370,680 , LOC100533722, 1168 more genes
    nsv4957658copy number variation1nstd200human GRCh38 chr7: 92,572,471-92,574,817 , GRCh37.p13 chr7: 92,201,785-92,204,131 FAM133B
    nsv4880762inversion1nstd200human GRCh37 chr7: 79,317,862-147,370,680 , GRCh38.p12 chr7: 79,688,546-147,673,588 , RN7SKP277, 1168 more genes
    nsv4763531inversion1nstd199human GRCh37 chr7: 66,769,373-102,019,339 , GRCh38.p12 chr7: 67,304,386-102,378,892 , ACHE, 578 more genes
    nsv4721485insertion1nstd186human GRCh37 chr7: 92,205,692-92,205,692 , GRCh38.p12 chr7: 92,576,378-92,576,378 FAM133B
    nsv4705627copy number variation1nstd195human GRCh37 chr7: 92,191,501-92,522,151 , GRCh38.p12 chr7: 92,562,187-92,892,837 CDK6, FAM133B, 4 more genes
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