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Items: 1 to 20 of 131

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv5493981copy number variation1nstd206human GRCh38 chr12: 71,698,723-71,698,839 , GRCh37.p13 chr12: 72,092,503-72,092,619 TMEM19
    nsv5124550mobile element insertion1nstd203human GRCh38 chr12: 71,694,537-71,694,548 , GRCh37.p13 chr12: 72,088,317-72,088,328 TMEM19
    nsv5037136inversion1nstd200human GRCh38 chr12: 69,787,024-109,882,221 , GRCh37.p13 chr12: 70,180,804-110,320,026 , RPL23AP68, 540 more genes
    nsv5036282inversion1nstd200human GRCh38 chr12: 52,338,357-95,425,642 , GRCh37.p13 chr12: 52,732,141-95,819,418 , MIR6502, 769 more genes
    nsv5032581inversion1nstd200human GRCh38 chr12: 67,763,754-90,678,993 , GRCh37.p13 chr12: 68,157,534-91,072,770 , LOC105369886, 255 more genes
    nsv5005949copy number variation1nstd200human GRCh38 chr12: 71,696,701-71,696,764 , GRCh37.p13 chr12: 72,090,481-72,090,544 TMEM19
    nsv4888823inversion1nstd200human GRCh37 chr12: 68,157,543-91,072,771 , GRCh38.p12 chr12: 67,763,763-90,678,994 , BEST3, 255 more genes
    nsv4886161inversion1nstd200human GRCh37 chr12: 70,180,810-110,320,027 , GRCh38.p12 chr12: 69,787,030-109,882,222 , LOC728739, 540 more genes
    nsv4883504inversion1nstd200human GRCh37 chr12: 52,732,141-95,819,418 , GRCh38.p12 chr12: 52,338,357-95,425,642 , MYL6B, 769 more genes
    nsv4755205inversion1nstd199human GRCh37 chr12: 25,956,127-125,801,151 , GRCh38.p12 chr12: 25,803,193-125,316,605 , ACACB, 1787 more genes
    nsv4736781copy number variation1nstd199human GRCh37 chr12: 25,957,322-125,801,148 , GRCh38.p12 chr12: 25,804,388-125,316,602 , RNA5SP368, 1787 more genes
    nsv4455767copy number variation1nstd102humanUncertain significance GRCh37 chr12: 71,081,550-73,526,446 , GRCh38.p12 chr12: 70,687,770-73,132,666 LOC105369832, LOC105369838, 17 more genes
    nsv4345788sequence alteration1nstd166human GRCh37.p13 chr12: 59,785,153-101,478,055 , GRCh38.p12 chr12: 59,391,372-101,084,277 , APAF1, 538 more genes
    nsv4325802inversion1nstd166human GRCh37.p13 chr12: 70,180,810-110,320,028 , GRCh38.p12 chr12: 69,787,030-109,882,223 , APAF1, 540 more genes
    nsv4324772inversion1nstd166human GRCh37.p13 chr12: 27,368,635-91,765,744 , GRCh38.p12 chr12: 27,215,702-91,371,967 , ATP2B1, 1101 more genes
    nsv4206454copy number variation1nstd166human GRCh37.p13 chr12: 72,079,451-72,079,503 , GRCh38.p12 chr12: 71,685,671-71,685,723 TMEM19
    nsv4198216copy number variation1nstd166human GRCh37.p13 chr12: 72,097,045-72,179,552 , GRCh38.p12 chr12: 71,703,265-71,785,772 TMEM19, LOC107984530, 1 more genes
    nsv4195224copy number variation1nstd166human GRCh37.p13 chr12: 72,080,717-72,081,336 , GRCh38.p12 chr12: 71,686,937-71,687,556 TMEM19
    nsv3924723copy number variation1nstd102humanPathogenic GRCh37 chr12: 70,163,517-77,357,997 , NCBI36 chr12: 68,449,784-75,882,128 , GRCh38 chr12: 69,769,737-76,964,217 KRR1, RNU4-65P, 80 more genes
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