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Items: 1 to 20 of 133

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5554634sequence alteration1nstd206human GRCh38 chr12: 108,320,077-108,322,553 , GRCh37.p13 chr12: 108,713,854-108,716,330 CMKLR1
    nsv5121687mobile element insertion1nstd203human GRCh38 chr12: 108,304,438-108,304,454 , GRCh37.p13 chr12: 108,698,215-108,698,231 CMKLR1
    nsv5037136inversion1nstd200human GRCh38 chr12: 69,787,024-109,882,221 , GRCh37.p13 chr12: 70,180,804-110,320,026 , RPL23AP68, 540 more genes
    nsv4993650copy number variation1nstd200human GRCh38 chr12: 107,479,304-108,313,763 , GRCh37.p13 chr12: 107,873,081-108,707,540 LOC105369963, CMKLR1, 14 more genes
    nsv4886161inversion1nstd200human GRCh37 chr12: 70,180,810-110,320,027 , GRCh38.p12 chr12: 69,787,030-109,882,222 , LOC728739, 540 more genes
    nsv4837486copy number variation1nstd200human GRCh37 chr12: 108,705,469-108,705,578 , GRCh38.p12 chr12: 108,311,692-108,311,801 CMKLR1
    nsv4769383copy number variation1nstd102humanUncertain significance GRCh37 chr12: 107,197,584-109,830,564 , GRCh38.p12 chr12: 106,803,806-109,392,759 TMEM263, MYO1H, 50 more genes
    nsv4756208inversion1nstd199human GRCh37 chr12: 104,359,633-125,801,147 , GRCh38.p12 chr12: 103,965,855-125,316,601 , ACACB, 453 more genes
    nsv4755205inversion1nstd199human GRCh37 chr12: 25,956,127-125,801,151 , GRCh38.p12 chr12: 25,803,193-125,316,605 , ACACB, 1787 more genes
    nsv4754840inversion1nstd199human GRCh37 chr12: 104,382,539-125,801,164 , GRCh38.p12 chr12: 103,988,761-125,316,618 , ACACB, 452 more genes
    nsv4749953copy number variation1nstd199human GRCh37 chr12: 108,716,006-108,716,377 , GRCh38.p12 chr12: 108,322,229-108,322,600 CMKLR1
    nsv4736781copy number variation1nstd199human GRCh37 chr12: 25,957,322-125,801,148 , GRCh38.p12 chr12: 25,804,388-125,316,602 , RNA5SP368, 1787 more genes
    nsv4728881copy number variation1nstd102humanPathogenic GRCh37 chr12: 106,498,814-112,252,906 , GRCh38.p12 chr12: 106,105,036-111,815,102 ATP2A2, CUX2, 115 more genes
    nsv4508350mobile element insertion1nstd166human GRCh37.p13 chr12: 108,697,476-108,697,476 , GRCh38.p12 chr12: 108,303,699-108,303,699 CMKLR1
    nsv4325802inversion1nstd166human GRCh37.p13 chr12: 70,180,810-110,320,028 , GRCh38.p12 chr12: 69,787,030-109,882,223 , APAF1, 540 more genes
    nsv4224564copy number variation1nstd166human GRCh37.p13 chr12: 108,727,486-108,732,274 , GRCh38.p12 chr12: 108,333,709-108,338,497 CMKLR1
    nsv4212936copy number variation1nstd166human GRCh37.p13 chr12: 108,659,558-108,755,934 , GRCh38.p12 chr12: 108,265,781-108,362,157 LOC196469, CMKLR1
    nsv3924338copy number variation1nstd102humanPathogenic NCBI36 chr12: 89,962,226-108,055,398 , GRCh38 chr12: 91,044,318-109,133,210 , GRCh37 chr12: 91,438,095-109,571,015 NUP37, TTC41P, 295 more genes
    nsv3922307copy number variation1nstd102humanUncertain significance NCBI36 chr12: 107,235,550-107,537,319 , GRCh37.p13 chr12: 108,711,420-109,013,190 , GRCh38.p12 chr12: 108,317,643-108,619,414 ISCU, FICD, 4 more genes
    nsv3919676copy number variation1nstd102humanUncertain significance NCBI36 chr12: 104,562,875-107,917,026 , GRCh37 chr12: 106,038,745-109,432,645 , GRCh38 chr12: 105,644,967-108,994,840 SELPLG, MTERF2, 54 more genes
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