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Items: 1 to 20 of 143

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5904716copy number variation1nstd209human GRCh38 chr5: 151,060,102-151,060,176 , GRCh37.p13 chr5: 150,439,663-150,439,737 TNIP1
    nsv5687891mobile element insertion2nstd211human GRCh38 chr5: 151,047,081-151,047,081 , GRCh37.p13 chr5: 150,426,642-150,426,642 TNIP1
    nsv5572948copy number variation1nstd207human GRCh38 chr5: 151,059,802-151,059,853 , GRCh37.p13 chr5: 150,439,363-150,439,414 TNIP1
    nsv5468987copy number variation1nstd206human GRCh38 chr5: 151,040,043-151,040,110 , GRCh37.p13 chr5: 150,419,604-150,419,671 TNIP1
    nsv5409073mobile element insertion1nstd206human GRCh38 chr5: 151,047,081-151,047,132 , GRCh37.p13 chr5: 150,426,642-150,426,693 TNIP1
    nsv5362544translocation1nstd200human GRCh38 chr5: 151,040,110-151,040,110 , GRCh38 chr5: 151,040,043-151,040,043 , GRCh37.p13 chr5: 150,419,604-150,419,604 , GRCh37.p13 chr5: 150,419,671-150,419,671 TNIP1
    nsv5226448copy number variation1nstd204human GRCh38.p13 chr5: 151,049,072-151,050,271 , GRCh37.p13 chr5: 150,428,633-150,429,832 TNIP1
    nsv5082995mobile element insertion1nstd203human GRCh38 chr5: 151,047,065-151,047,081 , GRCh37.p13 chr5: 150,426,626-150,426,642 TNIP1
    nsv5036421inversion1nstd200human GRCh38 chr5: 85,193,812-162,906,830 , GRCh37.p13 chr5: 84,489,630-162,333,836 , PRR16, 1116 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
    nsv4939202copy number variation1nstd200human GRCh38 chr5: 151,066,999-151,067,185 , GRCh37.p13 chr5: 150,446,560-150,446,746 TNIP1
    nsv4885569inversion1nstd200human GRCh37 chr5: 84,489,636-162,333,841 , GRCh38.p12 chr5: 85,193,818-162,906,835 , UBE2B, 1116 more genes
    nsv4592579copy number variation1nstd183human GRCh37 chr5: 150,462,467-150,471,621 , GRCh38.p12 chr5: 151,082,906-151,092,060 TNIP1
    nsv4555633insertion1nstd166human GRCh37.p13 chr5: 150,461,900-150,461,900 , GRCh38.p12 chr5: 151,082,339-151,082,339 TNIP1
    nsv4522279copy number variation1nstd166human GRCh37.p13 chr5: 150,413,755-150,414,141 , GRCh38.p12 chr5: 151,034,194-151,034,580 TNIP1
    nsv4488722mobile element insertion1nstd166human GRCh37.p13 chr5: 150,426,626-150,426,626 , GRCh38.p12 chr5: 151,047,065-151,047,065 TNIP1
    nsv4486829mobile element insertion1nstd166human GRCh37.p13 chr5: 150,428,685-150,428,685 , GRCh38.p12 chr5: 151,049,124-151,049,124 TNIP1
    nsv4378871copy number variation1nstd173human GRCh37 chr5: 150,420,056-150,491,349 , GRCh38.p12 chr5: 151,040,495-151,111,788 ANXA6, TNIP1
    nsv4128419copy number variation1nstd166human GRCh37.p13 chr5: 150,462,544-150,471,967 , GRCh38.p12 chr5: 151,082,983-151,092,406 TNIP1
    nsv4125875copy number variation1nstd166human GRCh37.p13 chr5: 150,460,502-150,460,576 , GRCh38.p12 chr5: 151,080,941-151,081,015 TNIP1
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