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Items: 1 to 20 of 98

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5932661copy number variation1nstd209human GRCh38 chr12: 109,090,575-109,090,682 , GRCh37.p13 chr12: 109,528,380-109,528,487 ALKBH2
    nsv5037136inversion1nstd200human GRCh38 chr12: 69,787,024-109,882,221 , GRCh37.p13 chr12: 70,180,804-110,320,026 , RPL23AP68, 540 more genes
    nsv4993660copy number variation1nstd200human GRCh38 chr12: 109,063,696-109,158,618 , GRCh37.p13 chr12: 109,501,501-109,596,423 ALKBH2, LOC105369974, 3 more genes
    nsv4886161inversion1nstd200human GRCh37 chr12: 70,180,810-110,320,027 , GRCh38.p12 chr12: 69,787,030-109,882,222 , LOC728739, 540 more genes
    nsv4835223copy number variation1nstd200human GRCh37 chr12: 109,501,500-109,596,424 , GRCh38.p12 chr12: 109,063,695-109,158,619 ACACB, USP30, 3 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
    nsv4675412copy number variation1nstd102humanUncertain significance GRCh37 chr12: 109,199,902-110,267,493 , GRCh38.p12 chr12: 108,806,126-109,829,688 FAM222A-AS1, LINC01486, 24 more genes
    nsv4607019copy number variation1nstd183human GRCh37 chr12: 109,502,441-109,597,157 , GRCh38.p12 chr12: 109,064,636-109,159,352 ACACB, ALKBH2, 3 more genes
    nsv4601853copy number variation1nstd183human GRCh37 chr12: 109,505,222-109,591,460 , GRCh38.p12 chr12: 109,067,417-109,153,655 ALKBH2, ACACB, 3 more genes
    nsv4455641copy number variation1nstd102humanUncertain significance GRCh37 chr12: 109,502,471-109,595,474 , GRCh38.p12 chr12: 109,064,666-109,157,669 USP30, LOC105369974, 3 more genes
    nsv4455358copy number variation1nstd102humanUncertain significance GRCh37 chr12: 109,501,323-109,603,494 , GRCh38.p12 chr12: 109,063,518-109,165,689 LOC105369974, UNG, 3 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
    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
    nsv3917474copy number variation1nstd102humanLikely benign GRCh37 chr12: 109,519,130-109,592,746 , GRCh38 chr12: 109,081,325-109,154,941 , NCBI36 chr12: 108,003,513-108,077,129 LOC105369974, UNG, 3 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
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