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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5913867copy number variation1nstd209human GRCh38 chr9: 69,710,239-69,711,706 , GRCh37.p13 chr9: 72,325,155-72,326,622 PTAR1
    nsv5850898copy number variation1nstd209human GRCh38 chr9: 69,710,356-69,711,655 , GRCh37.p13 chr9: 72,325,272-72,326,571 PTAR1
    nsv5724678mobile element insertion1nstd211human GRCh38 chr9: 69,710,858-69,710,858 , GRCh37.p13 chr9: 72,325,774-72,325,774 PTAR1
    nsv5719043mobile element insertion1nstd211human GRCh38 chr9: 69,710,870-69,710,870 , GRCh37.p13 chr9: 72,325,786-72,325,786 PTAR1
    nsv5707767mobile element insertion2nstd211human GRCh38 chr9: 69,743,371-69,743,371 , GRCh37.p13 chr9: 72,358,287-72,358,287 PTAR1
    nsv5490190copy number variation1nstd206human GRCh38 chr9: 69,718,686-69,723,324 , GRCh37.p13 chr9: 72,333,602-72,338,240 PTAR1
    nsv5488811copy number variation1nstd206human GRCh38 chr9: 69,724,580-69,724,672 , GRCh37.p13 chr9: 72,339,496-72,339,588 PTAR1
    nsv5487177copy number variation1nstd206human GRCh38 chr9: 69,708,714-69,708,773 , GRCh37.p13 chr9: 72,323,630-72,323,689 PTAR1
    nsv5484286copy number variation1nstd206human GRCh38 chr9: 69,708,552-69,718,552 , GRCh37.p13 chr9: 72,323,468-72,333,468 PTAR1
    nsv5481117copy number variation1nstd206human GRCh38 chr9: 69,710,242-69,711,717 , GRCh37.p13 chr9: 72,325,158-72,326,633 PTAR1
    nsv5478607copy number variation1nstd206human GRCh38 chr9: 69,756,771-69,766,543 , GRCh37.p13 chr9: 72,371,687-72,381,459 LOC105376076, PTAR1
    nsv5474816copy number variation1nstd206human GRCh38 chr9: 69,720,692-69,720,758 , GRCh37.p13 chr9: 72,335,608-72,335,674 PTAR1
    nsv5397237mobile element insertion1nstd206human GRCh38 chr9: 69,743,371-69,743,422 , GRCh37.p13 chr9: 72,358,287-72,358,338 PTAR1
    nsv5316172copy number variation1nstd204human GRCh38.p13 chr9: 69,578,731-69,816,086 , GRCh37.p13 chr9: 72,193,647-72,431,002 LOC105376076, APBA1, 1 more genes
    nsv5254904copy number variation1nstd204human GRCh38.p13 chr9: 69,578,701-69,816,100 , GRCh37.p13 chr9: 72,193,617-72,431,016 PTAR1, LOC105376076, 1 more genes
    nsv5244332copy number variation1nstd204human GRCh38.p13 chr9: 69,717,906-69,758,642 , GRCh37.p13 chr9: 72,332,822-72,373,558 PTAR1, LOC105376076
    nsv5198179mobile element insertion1nstd203human GRCh38 chr9: 69,710,858-69,710,870 , GRCh37.p13 chr9: 72,325,774-72,325,786 PTAR1
    nsv5127063mobile element insertion1nstd203human GRCh38 chr9: 69,717,986-69,717,995 , GRCh37.p13 chr9: 72,332,902-72,332,911 PTAR1
    nsv4968288copy number variation1nstd200human GRCh38 chr9: 69,728,588-69,730,655 , GRCh37.p13 chr9: 72,343,504-72,345,571 PTAR1
    nsv4954804copy number variation1nstd200human GRCh38 chr9: 69,756,771-69,766,543 , GRCh37.p13 chr9: 72,371,687-72,381,459 LOC105376076, PTAR1
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