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Items: 1 to 20 of 137

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7074641inversion1nstd229human GRCh38 chr12: 52,659,002-59,632,575 , GRCh37.p13 chr12: 53,052,786-60,026,356 , LOC105369777, 292 more genes
    nsv7071931inversion1nstd229human GRCh38 chr12: 55,156,710-64,781,897 , GRCh37.p13 chr12: 55,550,494-65,175,677 ZBTB39, MIR548Z, 236 more genes
    nsv7065167inversion1nstd229human GRCh38 chr12: 55,524,684-56,392,713 , GRCh37.p13 chr12: 55,918,468-56,786,497 TMEM198B, BLOC1S1, 57 more genes
    nsv7060060inversion1nstd229human GRCh38 chr12: 55,500,913-56,344,820 , GRCh37.p13 chr12: 55,894,697-56,738,604 MYL6B, OR6C64P, 54 more genes
    nsv6924218copy number variation1nstd229human GRCh38 chr12: 55,714,201-56,819,900 , GRCh37.p13 chr12: 56,107,985-57,213,684 ESYT1, STAT2, 66 more genes
    nsv6588914inversion1nstd223human GRCh38 chr12: 55,524,684-56,392,758 , GRCh37.p13 chr12: 55,918,468-56,786,542 IL23A, RPL41, 57 more genes
    nsv6315199copy number variation1nstd102humanUncertain significance GRCh38 chr12: 55,986,511-56,885,590 , GRCh37.p13 chr12: 56,380,295-57,279,374 ERBB3, APOF, 47 more genes
    nsv6313979copy number variation1nstd102humanUncertain significance GRCh37 chr12: 56,333,262-57,010,442 , GRCh38.p12 chr12: 55,939,478-56,616,658 TRS-CGA4-1, ANKRD52, 42 more genes
    nsv6143026copy number variation1nstd206human GRCh38 chr12: 48,500,915-111,724,058 , GRCh37.p13 chr12: 48,894,698-112,161,862 , LINC00592, 1206 more genes
    nsv6132699copy number variation1nstd213human GRCh37 chr12: 56,390,000-56,610,001 , GRCh38.p12 chr12: 55,996,216-56,216,217 MYL6, RPS26, 15 more genes
    nsv5712309mobile element insertion1nstd211human GRCh38 chr12: 56,103,507-56,103,507 , GRCh37.p13 chr12: 56,497,291-56,497,291 ERBB3, PA2G4, 1 more genes
    nsv5695318mobile element insertion1nstd211human GRCh38 chr12: 56,113,876-56,113,876 , GRCh37.p13 chr12: 56,507,660-56,507,660 PA2G4
    nsv5420220mobile element insertion1nstd206human GRCh38 chr12: 56,113,876-56,113,882 , GRCh37.p13 chr12: 56,507,660-56,507,666 PA2G4
    nsv5419943mobile element insertion1nstd206human GRCh38 chr12: 56,103,507-56,103,558 , GRCh37.p13 chr12: 56,497,291-56,497,342 ERBB3, PA2G4, 1 more genes
    nsv5280254copy number variation1nstd204human GRCh38.p13 chr12: 56,102,865-56,103,864 , GRCh37.p13 chr12: 56,496,649-56,497,648 LOC105369782, PA2G4, 1 more genes
    nsv5278526copy number variation1nstd204human GRCh38.p13 chr12: 55,839,801-56,299,500 , GRCh37.p13 chr12: 56,233,585-56,693,284 , NABP2, 30 more genes
    nsv5273203copy number variation1nstd204human GRCh38.p13 chr12: 56,108,477-56,109,479 , GRCh37.p13 chr12: 56,502,261-56,503,263 PA2G4
    nsv5040224inversion1nstd200human GRCh38 chr12: 47,213,128-71,357,206 , GRCh37.p13 chr12: 47,606,911-71,750,986 , NR4A1, 686 more genes
    nsv5036282inversion1nstd200human GRCh38 chr12: 52,338,357-95,425,642 , GRCh37.p13 chr12: 52,732,141-95,819,418 , MIR6502, 769 more genes
    nsv4883504inversion1nstd200human GRCh37 chr12: 52,732,141-95,819,418 , GRCh38.p12 chr12: 52,338,357-95,425,642 , MYL6B, 769 more genes
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