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Items: 1 to 20 of 287

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5974917insertion1nstd209human GRCh38 chr12: 79,639,881-79,639,881 , GRCh37.p13 chr12: 80,033,661-80,033,661 PAWR
    nsv5940561copy number variation1nstd209human GRCh38 chr12: 79,671,623-79,676,824 , GRCh37.p13 chr12: 80,065,403-80,070,604 PAWR
    nsv5936253copy number variation1nstd209human GRCh38 chr12: 79,688,956-79,689,589 , GRCh37.p13 chr12: 80,082,736-80,083,369 PAWR
    nsv5855573copy number variation1nstd209human GRCh38 chr12: 79,671,631-79,674,368 , GRCh37.p13 chr12: 80,065,411-80,068,148 PAWR
    nsv5852398copy number variation1nstd209human GRCh38 chr12: 79,672,156-79,676,068 , GRCh37.p13 chr12: 80,065,936-80,069,848 PAWR
    nsv5725483mobile element insertion2nstd211human GRCh38 chr12: 79,612,630-79,612,630 , GRCh37.p13 chr12: 80,006,410-80,006,410 PAWR
    nsv5725336mobile element insertion1nstd211human GRCh38 chr12: 79,623,816-79,623,816 , GRCh37.p13 chr12: 80,017,596-80,017,596 PAWR
    nsv5707137mobile element insertion2nstd211human GRCh38 chr12: 79,637,557-79,637,557 , GRCh37.p13 chr12: 80,031,337-80,031,337 PAWR
    nsv5699337mobile element insertion2nstd211human GRCh38 chr12: 79,590,614-79,590,614 , GRCh37.p13 chr12: 79,984,394-79,984,394 PAWR
    nsv5659035insertion1nstd207human GRCh38 chr12: 79,612,617-79,612,617 , GRCh37.p13 chr12: 80,006,397-80,006,397 PAWR
    nsv5658258insertion1nstd207human GRCh38 chr12: 79,639,881-79,639,881 , GRCh37.p13 chr12: 80,033,661-80,033,661 PAWR
    nsv5600755copy number variation1nstd207human GRCh38 chr12: 79,632,307-79,632,368 , GRCh37.p13 chr12: 80,026,087-80,026,148 PAWR
    nsv5593303copy number variation1nstd207human GRCh38 chr12: 79,613,943-79,613,999 , GRCh37.p13 chr12: 80,007,723-80,007,779 PAWR
    nsv5513617copy number variation1nstd206human GRCh38 chr12: 79,683,304-79,683,443 , GRCh37.p13 chr12: 80,077,084-80,077,223 PAWR
    nsv5503826copy number variation1nstd206human GRCh38 chr12: 79,611,304-79,611,391 , GRCh37.p13 chr12: 80,005,084-80,005,171 PAWR
    nsv5502677copy number variation1nstd206human GRCh38 chr12: 79,688,956-79,689,593 , GRCh37.p13 chr12: 80,082,736-80,083,373 PAWR
    nsv5500934copy number variation1nstd206human GRCh38 chr12: 76,069,603-82,449,398 , GRCh37.p13 chr12: 76,463,383-82,843,177 , E2F7, 65 more genes
    nsv5500755copy number variation1nstd206human GRCh38 chr12: 79,579,999-79,583,920 , GRCh37.p13 chr12: 79,973,779-79,977,700 PAWR
    nsv5493936copy number variation1nstd206human GRCh38 chr12: 79,681,677-79,681,964 , GRCh37.p13 chr12: 80,075,457-80,075,744 PAWR
    nsv5430211mobile element insertion1nstd206human GRCh38 chr12: 79,637,557-79,637,608 , GRCh37.p13 chr12: 80,031,337-80,031,388 PAWR
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