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Items: 1 to 20 of 421

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6124736insertion1nstd186human GRCh37 chr12: 70,740,798-70,740,810 , GRCh38.p12 chr12: 70,347,018-70,347,030 CNOT2
    nsv6117357mobile element insertion1nstd186human GRCh37 chr12: 70,680,974-70,680,994 , GRCh38.p12 chr12: 70,287,194-70,287,214 CNOT2
    nsv6114937mobile element insertion1nstd186human GRCh37 chr12: 70,679,895-70,679,946 , GRCh38.p12 chr12: 70,286,115-70,286,166 CNOT2
    nsv6112755copy number variation1nstd102humanPathogenic GRCh37 chr12: 65,251,705-75,263,379 , GRCh38.p12 chr12: 64,857,925-74,869,599 LINC02421, TBC1D15, 144 more genes
    nsv5976908inversion1nstd209human GRCh38 chr12: 70,288,279-70,289,721 , GRCh37.p13 chr12: 70,682,059-70,683,501 CNOT2
    nsv5967636insertion1nstd209human GRCh38 chr12: 70,286,106-70,286,106 , GRCh37.p13 chr12: 70,679,886-70,679,886 CNOT2
    nsv5940029copy number variation1nstd209human GRCh38 chr12: 70,264,312-70,264,367 , GRCh37.p13 chr12: 70,658,092-70,658,147 CNOT2
    nsv5939506copy number variation1nstd209human GRCh38 chr12: 70,281,816-70,281,865 , GRCh37.p13 chr12: 70,675,596-70,675,645 CNOT2
    nsv5939018copy number variation1nstd209human GRCh38 chr12: 70,304,219-70,304,291 , GRCh37.p13 chr12: 70,697,999-70,698,071 CNOT2
    nsv5852931copy number variation1nstd209human GRCh38 chr12: 70,287,194-70,288,293 , GRCh37.p13 chr12: 70,680,974-70,682,073 CNOT2
    nsv5713372mobile element insertion2nstd211human GRCh38 chr12: 70,321,807-70,321,807 , GRCh37.p13 chr12: 70,715,587-70,715,587 CNOT2
    nsv5708951mobile element insertion1nstd211human GRCh38 chr12: 70,287,194-70,287,194 , GRCh37.p13 chr12: 70,680,974-70,680,974 CNOT2
    nsv5707734mobile element insertion2nstd211human GRCh38 chr12: 70,286,115-70,286,115 , GRCh37.p13 chr12: 70,679,895-70,679,895 CNOT2
    nsv5701921mobile element insertion1nstd211human GRCh38 chr12: 70,339,167-70,339,167 , GRCh37.p13 chr12: 70,732,947-70,732,947 CNOT2
    nsv5696097mobile element insertion2nstd211human GRCh38 chr12: 70,307,593-70,307,593 , GRCh37.p13 chr12: 70,701,373-70,701,373 CNOT2
    nsv5661521insertion1nstd207human GRCh38 chr12: 70,288,278-70,288,278 , GRCh37.p13 chr12: 70,682,058-70,682,058 CNOT2
    nsv5649473insertion1nstd207human GRCh38 chr12: 70,281,816-70,281,816 , GRCh37.p13 chr12: 70,675,596-70,675,596 CNOT2
    nsv5645081insertion1nstd207human GRCh38 chr12: 70,286,106-70,286,106 , GRCh37.p13 chr12: 70,679,886-70,679,886 CNOT2
    nsv5598309copy number variation1nstd207human GRCh38 chr12: 70,286,114-70,288,118 , GRCh37.p13 chr12: 70,679,894-70,681,898 CNOT2
    nsv5534824insertion1nstd206human GRCh38 chr12: 70,347,018-70,347,030 , GRCh37.p13 chr12: 70,740,798-70,740,810 CNOT2
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