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Items: 1 to 20 of 220

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5972434inversion1nstd209human GRCh37.p13 chr5: 114,252,584-114,781,685 , GRCh38 chr5: 114,916,887-115,445,988 CTNNA1P1, PGGT1B, 7 more genes
    nsv5719175mobile element insertion2nstd211human GRCh38 chr5: 115,180,762-115,180,762 , GRCh37.p13 chr5: 114,516,459-114,516,459 TRIM36
    nsv5689308mobile element insertion1nstd211human GRCh38 chr5: 115,149,596-115,149,596 , GRCh37.p13 chr5: 114,485,293-114,485,293 TRIM36
    nsv5678725mobile element insertion1nstd211human GRCh38 chr5: 115,149,659-115,149,659 , GRCh37.p13 chr5: 114,485,356-114,485,356 TRIM36
    nsv5643790insertion1nstd207human GRCh38 chr5: 115,180,758-115,180,758 , GRCh37.p13 chr5: 114,516,455-114,516,455 TRIM36
    nsv5467247copy number variation1nstd206human GRCh38 chr5: 115,171,923-115,176,239 , GRCh37.p13 chr5: 114,507,620-114,511,936 TRIM36
    nsv5463138copy number variation1nstd206human GRCh38 chr5: 115,141,978-115,142,194 , GRCh37.p13 chr5: 114,477,675-114,477,891 TRIM36
    nsv5084865mobile element insertion1nstd203human GRCh38 chr5: 115,130,581-115,130,596 , GRCh37.p13 chr5: 114,466,278-114,466,293 TRIM36
    nsv5083253mobile element insertion1nstd203human GRCh38 chr5: 115,128,758-115,128,788 , GRCh37.p13 chr5: 114,464,455-114,464,485 TRIM36
    nsv5036421inversion1nstd200human GRCh38 chr5: 85,193,812-162,906,830 , GRCh37.p13 chr5: 84,489,630-162,333,836 , PRR16, 1116 more genes
    nsv5034346inversion1nstd200human GRCh38 chr5: 99,223,339-135,778,784 , GRCh37.p13 chr5: 98,559,043-135,114,473 , NUDT12, 438 more genes
    nsv4947215copy number variation1nstd200human GRCh38 chr5: 93,957,557-155,223,076 , GRCh37.p13 chr5: 93,293,262-154,602,636 , TGFBI, 937 more genes
    nsv4944943copy number variation1nstd200human GRCh38 chr5: 115,141,978-115,142,194 , GRCh37.p13 chr5: 114,477,675-114,477,891 TRIM36
    nsv4932402copy number variation1nstd200human GRCh38 chr5: 115,149,268-115,155,134 , GRCh37.p13 chr5: 114,484,965-114,490,831 TRIM36
    nsv4885569inversion1nstd200human GRCh37 chr5: 84,489,636-162,333,841 , GRCh38.p12 chr5: 85,193,818-162,906,835 , UBE2B, 1116 more genes
    nsv4872282inversion1nstd200human GRCh37 chr5: 98,106,197-132,803,784 , GRCh38.p12 chr5: 98,770,493-133,468,092 , LEAP2, 395 more genes
    nsv4805754copy number variation1nstd200human GRCh37 chr5: 114,477,675-114,477,891 , GRCh38.p12 chr5: 115,141,978-115,142,194 TRIM36
    nsv4803524copy number variation1nstd200human GRCh37 chr5: 114,512,641-114,513,487 , GRCh38.p12 chr5: 115,176,944-115,177,790 TRIM36
    nsv4803523copy number variation1nstd200human GRCh37 chr5: 114,484,965-114,490,831 , GRCh38.p12 chr5: 115,149,268-115,155,134 TRIM36
    nsv4597659copy number variation1nstd183human GRCh37 chr5: 114,459,620-114,461,452 , GRCh38.p12 chr5: 115,123,923-115,125,755 TRIM36
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