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Items: 1 to 20 of 107

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5356355translocation1nstd200human GRCh38 chr12: 108,596,451-108,596,451 , GRCh38 chr12: 108,596,349-108,596,349 , GRCh37.p13 chr12: 108,990,125-108,990,125 , GRCh37.p13 chr12: 108,990,227-108,990,227 TMEM119
    nsv5316389copy number variation1nstd204human GRCh38.p13 chr12: 108,598,058-108,598,266 , GRCh37.p13 chr12: 108,991,834-108,992,042 TMEM119
    nsv5037136inversion1nstd200human GRCh38 chr12: 69,787,024-109,882,221 , GRCh37.p13 chr12: 70,180,804-110,320,026 , RPL23AP68, 540 more genes
    nsv4886161inversion1nstd200human GRCh37 chr12: 70,180,810-110,320,027 , GRCh38.p12 chr12: 69,787,030-109,882,222 , LOC728739, 540 more genes
    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
    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
    nsv4325802inversion1nstd166human GRCh37.p13 chr12: 70,180,810-110,320,028 , GRCh38.p12 chr12: 69,787,030-109,882,223 , APAF1, 540 more genes
    nsv4223397copy number variation1nstd166human GRCh37.p13 chr12: 108,991,843-108,992,034 , GRCh38.p12 chr12: 108,598,067-108,598,258 TMEM119
    nsv4215950copy number variation1nstd166human GRCh37.p13 chr12: 108,990,125-108,990,227 , GRCh38.p12 chr12: 108,596,349-108,596,451 TMEM119
    nsv3969587insertion1nstd168human GRCh38 chr12: 108,532,048-108,592,871 , GRCh37.p13 chr12: 108,925,824-108,986,647 SART3, ISCU, 1 more genes
    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
    nsv3916234copy number variation1nstd102humanPathogenic NCBI36 chr12: 104,152,585-111,116,873 , GRCh37 chr12: 105,628,455-112,632,490 , GRCh38 chr12: 105,234,677-112,194,686 LOC100287944, PWP1, 141 more genes
    nsv3914194copy number variation1nstd102humanPathogenic NCBI36 chr12: 100,698-132,283,466 , GRCh37 chr12: 282,465-133,773,393 , GRCh38 chr12: 121,271-133,196,807 , BTG1P1, 2451 more genes
    nsv3905447copy number variation2nstd102humanPathogenic GRCh37 chr12: 173,787-133,777,902 , GRCh38.p12 chr12: 64,621-133,201,316 , LOH12CR2, 2452 more genes
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