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Items: 1 to 20 of 147

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5711772mobile element insertion1nstd211human GRCh38 chr12: 95,975,362-95,975,362 , GRCh37.p13 chr12: 96,369,140-96,369,140 HAL
    nsv5508129copy number variation1nstd206human GRCh38 chr12: 95,990,892-96,016,728 , GRCh37.p13 chr12: 96,384,670-96,410,506 LOC102723340, LTA4H, 1 more genes
    nsv5133310mobile element insertion1nstd203human GRCh38 chr12: 95,976,887-95,976,899 , GRCh37.p13 chr12: 96,370,665-96,370,677 HAL
    nsv5132354mobile element insertion1nstd203human GRCh38 chr12: 95,976,889-95,976,899 , GRCh37.p13 chr12: 96,370,667-96,370,677 HAL
    nsv5037136inversion1nstd200human GRCh38 chr12: 69,787,024-109,882,221 , GRCh37.p13 chr12: 70,180,804-110,320,026 , RPL23AP68, 540 more genes
    nsv4993589copy number variation1nstd200human GRCh38 chr12: 95,990,861-96,016,763 , GRCh37.p13 chr12: 96,384,639-96,410,541 HAL, LTA4H, 1 more genes
    nsv4993588copy number variation1nstd200human GRCh38 chr12: 95,990,904-96,003,966 , GRCh37.p13 chr12: 96,384,682-96,397,744 LTA4H, LOC102723340, 1 more genes
    nsv4886161inversion1nstd200human GRCh37 chr12: 70,180,810-110,320,027 , GRCh38.p12 chr12: 69,787,030-109,882,222 , LOC728739, 540 more genes
    nsv4830541copy number variation1nstd200human GRCh37 chr12: 96,384,682-96,397,744 , GRCh38.p12 chr12: 95,990,904-96,003,966 LTA4H, LOC102723340, 1 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
    nsv4613132copy number variation1nstd183human GRCh37 chr12: 96,389,996-96,410,317 , GRCh38.p12 chr12: 95,996,218-96,016,539 LTA4H, HAL, 1 more genes
    nsv4609164copy number variation1nstd183human GRCh37 chr12: 96,387,658-96,387,905 , GRCh38.p12 chr12: 95,993,880-95,994,127 HAL
    nsv4599922copy number variation1nstd183human GRCh37 chr12: 96,387,595-96,387,717 , GRCh38.p12 chr12: 95,993,817-95,993,939 HAL
    nsv4503970mobile element insertion1nstd166human GRCh37.p13 chr12: 96,370,665-96,370,665 , GRCh38.p12 chr12: 95,976,887-95,976,887 HAL
    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
    nsv4224971copy number variation1nstd166human GRCh37.p13 chr12: 96,367,645-96,367,735 , GRCh38.p12 chr12: 95,973,867-95,973,957 HAL
    nsv4224009copy number variation1nstd166human GRCh37.p13 chr12: 96,384,692-96,410,506 , GRCh38.p12 chr12: 95,990,914-96,016,728 HAL, LOC102723340, 1 more genes
    nsv4221348copy number variation1nstd166human GRCh37.p13 chr12: 96,388,956-96,389,085 , GRCh38.p12 chr12: 95,995,178-95,995,307 HAL, LOC102723340
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