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Items: 1 to 20 of 135

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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
    nsv6935316copy number variation1nstd229human GRCh38 chr12: 55,940,075-55,958,823 , GRCh37.p13 chr12: 56,333,859-56,352,607 PMEL, DGKA
    nsv6928552copy number variation1nstd229human GRCh38 chr12: 55,958,608-55,961,315 , GRCh37.p13 chr12: 56,352,392-56,355,099 PMEL
    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
    nsv6637639copy number variation1nstd102humanUncertain significance GRCh37 chr12: 56,056,806-56,438,901 , GRCh38.p12 chr12: 55,663,022-56,045,117 DGKA, PYM1, 24 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
    nsv6585341inversion1nstd223human GRCh38 chr12: 55,960,561-55,961,248 , GRCh37.p13 chr12: 56,354,345-56,355,032 PMEL
    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
    nsv6084837insertion1nstd212human GRCh38 chr12: 55,955,863-55,955,863 , GRCh37.p13 chr12: 56,349,647-56,349,647 PMEL
    nsv5561337sequence alteration1nstd206human GRCh38 chr12: 55,959,668-55,959,760 , GRCh37.p13 chr12: 56,353,452-56,353,544 PMEL
    nsv5502247copy number variation1nstd206human GRCh38 chr12: 55,958,880-55,959,041 , GRCh37.p13 chr12: 56,352,664-56,352,825 PMEL
    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
    nsv5275142copy number variation1nstd204human GRCh38.p13 chr12: 55,960,593-55,962,861 , GRCh37.p13 chr12: 56,354,377-56,356,645 PMEL
    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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