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Items: 1 to 20 of 207

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5978543insertion1nstd209human GRCh38 chr12: 126,005,608-126,005,608 , GRCh37.p13 chr12: 126,490,154-126,490,154 LINC02826
    nsv5852845copy number variation1nstd209human GRCh38 chr12: 126,008,819-126,012,908 , GRCh37.p13 chr12: 126,493,365-126,497,454 LINC02826
    nsv5711130mobile element insertion1nstd211human GRCh38 chr12: 126,004,979-126,004,979 , GRCh37.p13 chr12: 126,489,525-126,489,525 LINC02826
    nsv5709957mobile element insertion2nstd211human GRCh38 chr12: 125,995,261-125,995,261 , GRCh37.p13 chr12: 126,479,807-126,479,807 LOC105370058, LINC02826
    nsv5705592mobile element insertion2nstd211human GRCh38 chr12: 126,018,412-126,018,412 , GRCh37.p13 chr12: 126,502,958-126,502,958 LINC02826, LOC105370056
    nsv5513387copy number variation1nstd206human GRCh38 chr12: 126,041,597-126,041,794 , GRCh37.p13 chr12: 126,526,143-126,526,340 LINC02826
    nsv5419644mobile element insertion1nstd206human GRCh38 chr12: 125,995,261-125,995,312 , GRCh37.p13 chr12: 126,479,807-126,479,858 LINC02826, LOC105370058
    nsv5417667mobile element insertion1nstd206human GRCh38 chr12: 126,004,979-126,005,030 , GRCh37.p13 chr12: 126,489,525-126,489,576 LINC02826
    nsv5417558mobile element insertion1nstd206human GRCh38 chr12: 126,018,412-126,018,463 , GRCh37.p13 chr12: 126,502,958-126,503,009 LOC105370056, LINC02826
    nsv5381782copy number variation1nstd102humanPathogenic GRCh37 chr12: 123,878,845-126,829,341 , GRCh38.p12 chr12: 123,394,298-126,344,795 DDX55, ZNF664, 55 more genes
    nsv5133904mobile element insertion1nstd203human GRCh38 chr12: 125,995,249-125,995,261 , GRCh37.p13 chr12: 126,479,795-126,479,807 LOC105370058, LINC02826
    nsv5125972mobile element insertion1nstd203human GRCh38 chr12: 126,018,398-126,018,412 , GRCh37.p13 chr12: 126,502,944-126,502,958 LOC105370056, LINC02826
    nsv5122472mobile element insertion1nstd203human GRCh38 chr12: 125,995,261-125,995,261 , GRCh37.p13 chr12: 126,479,807-126,479,807 LINC02826, LOC105370058
    nsv5120091mobile element insertion1nstd203human GRCh38 chr12: 126,005,608-126,005,634 , GRCh37.p13 chr12: 126,490,154-126,490,180 LINC02826
    nsv5006249copy number variation1nstd200human GRCh38 chr12: 126,018,725-126,021,927 , GRCh37.p13 chr12: 126,503,271-126,506,473 LINC02826, LOC105370056
    nsv5006248copy number variation1nstd200human GRCh38 chr12: 126,005,575-126,005,699 , GRCh37.p13 chr12: 126,490,121-126,490,245 LINC02826
    nsv4993847copy number variation1nstd200human GRCh38 chr12: 126,032,740-126,418,205 , GRCh37.p13 chr12: 126,517,286-126,902,751 , LOC105379613, 7 more genes
    nsv4993846copy number variation1nstd200human GRCh38 chr12: 125,985,681-126,044,865 , GRCh37.p13 chr12: 126,470,227-126,529,411 LOC105370056, LINC02826, 1 more genes
    nsv4838001copy number variation1nstd200human GRCh37 chr12: 126,474,592-126,474,812 , GRCh38.p12 chr12: 125,990,046-125,990,266 LINC02826
    nsv4565623mobile element insertion1nstd166human GRCh37.p13 chr12: 126,510,526-126,510,526 , GRCh38.p12 chr12: 126,025,980-126,025,980 LINC02826, LOC105370056
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