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Items: 1 to 20 of 275

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6119657copy number variation1nstd186human GRCh37 chr5: 147,553,039-147,554,775 , GRCh38.p12 chr5: 148,173,476-148,175,212 SPINK14
    nsv5971661inversion1nstd209human GRCh38 chr5: 148,175,214-148,175,752 , GRCh37.p13 chr5: 147,554,777-147,555,315 SPINK14
    nsv5967976inversion1nstd209human GRCh38 chr5: 148,173,476-148,175,051 , GRCh37.p13 chr5: 147,553,039-147,554,614 SPINK14
    nsv5959165insertion1nstd209human GRCh38 chr5: 148,173,138-148,173,138 , GRCh37.p13 chr5: 147,552,701-147,552,701 SPINK14
    nsv5906631copy number variation1nstd209human GRCh38 chr5: 148,173,620-148,175,046 , GRCh37.p13 chr5: 147,553,183-147,554,609 SPINK14
    nsv5904848copy number variation1nstd209human GRCh38 chr5: 148,173,552-148,175,121 , GRCh37.p13 chr5: 147,553,115-147,554,684 SPINK14
    nsv5674907mobile element insertion2nstd211human GRCh38 chr5: 148,173,153-148,173,153 , GRCh37.p13 chr5: 147,552,716-147,552,716 SPINK14
    nsv5642317insertion1nstd207human GRCh38 chr5: 148,173,474-148,173,474 , GRCh37.p13 chr5: 147,553,037-147,553,037 SPINK14
    nsv5564970copy number variation1nstd207human GRCh38 chr5: 148,173,527-148,175,210 , GRCh37.p13 chr5: 147,553,090-147,554,773 SPINK14
    nsv5556321sequence alteration1nstd206human GRCh38 chr5: 148,173,476-148,175,215 , GRCh37.p13 chr5: 147,553,039-147,554,778 SPINK14
    nsv5462857copy number variation1nstd206human GRCh38 chr5: 148,173,445-148,175,244 , GRCh37.p13 chr5: 147,553,008-147,554,807 SPINK14
    nsv5457815copy number variation1nstd206human GRCh38 chr5: 148,021,659-148,360,000 , GRCh37.p13 chr5: 147,401,222-147,739,563 PGBD4P3, SPINK14, 8 more genes
    nsv5398222mobile element insertion1nstd206human GRCh38 chr5: 148,173,153-148,173,204 , GRCh37.p13 chr5: 147,552,716-147,552,767 SPINK14
    nsv5388556copy number variation1nstd186human GRCh37 chr5: 147,553,038-147,554,778 , GRCh38.p12 chr5: 148,173,475-148,175,215 SPINK14
    nsv5387201copy number variation1nstd186human GRCh37 chr5: 147,553,039-147,554,776 , GRCh38.p12 chr5: 148,173,476-148,175,213 SPINK14
    nsv5343829translocation1nstd200human GRCh37 chr5: 147,554,779-147,554,779 , GRCh37 chr5: 147,554,240-147,554,240 , GRCh38.p12 chr5: 148,174,677-148,174,677 , GRCh38.p12 chr5: 148,175,216-148,175,216 SPINK14
    nsv5333142translocation1nstd200human GRCh37 chr5: 147,553,039-147,553,039 , GRCh37 chr5: 147,554,606-147,554,606 , GRCh38.p12 chr5: 148,175,043-148,175,043 , GRCh38.p12 chr5: 148,173,476-148,173,476 SPINK14
    nsv5329512translocation1nstd204human GRCh38.p13 chr5: 148,173,476-148,173,476 , GRCh38.p13 chr5: 148,175,043-148,175,043 , GRCh37.p13 chr5: 147,553,039-147,553,039 , GRCh37.p13 chr5: 147,554,606-147,554,606 SPINK14
    nsv5328902translocation1nstd204human GRCh38.p13 chr5: 148,175,216-148,175,216 , GRCh38.p13 chr5: 148,174,677-148,174,677 , GRCh37.p13 chr5: 147,554,240-147,554,240 , GRCh37.p13 chr5: 147,554,779-147,554,779 SPINK14
    nsv5317285copy number variation1nstd204human GRCh38.p13 chr5: 148,173,468-148,175,224 , GRCh37.p13 chr5: 147,553,031-147,554,787 SPINK14
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