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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
    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
    nsv5501097copy number variation1nstd206human GRCh38 chr12: 96,032,847-96,034,168 , GRCh37.p13 chr12: 96,426,625-96,427,946 LTA4H, TRD-GTC2-8
    nsv5129705mobile element insertion1nstd203human GRCh38 chr12: 96,016,340-96,016,360 , GRCh37.p13 chr12: 96,410,118-96,410,138 LTA4H
    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
    nsv4989950copy number variation1nstd200human GRCh38 chr12: 96,041,495-96,041,572 , GRCh37.p13 chr12: 96,435,273-96,435,350 LTA4H
    nsv4989949copy number variation1nstd200human GRCh38 chr12: 96,032,847-96,034,168 , GRCh37.p13 chr12: 96,426,625-96,427,946 TRD-GTC2-8, LTA4H
    nsv4989948copy number variation1nstd200human GRCh38 chr12: 96,026,130-96,026,834 , GRCh37.p13 chr12: 96,419,908-96,420,612 LTA4H
    nsv4886161inversion1nstd200human GRCh37 chr12: 70,180,810-110,320,027 , GRCh38.p12 chr12: 69,787,030-109,882,222 , LOC728739, 540 more genes
    nsv4847616copy number variation1nstd200human GRCh37 chr12: 96,426,625-96,427,946 , GRCh38.p12 chr12: 96,032,847-96,034,168 TRD-GTC2-8, LTA4H
    nsv4834635copy number variation1nstd200human GRCh37 chr12: 96,419,908-96,420,612 , GRCh38.p12 chr12: 96,026,130-96,026,834 LTA4H
    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
    nsv4571660mobile element insertion1nstd166human GRCh37.p13 chr12: 96,415,452-96,415,452 , GRCh38.p12 chr12: 96,021,674-96,021,674 LTA4H
    nsv4512633mobile element insertion1nstd166human GRCh37.p13 chr12: 96,403,154-96,403,154 , GRCh38.p12 chr12: 96,009,376-96,009,376 LTA4H, LOC102723340
    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
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