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Items: 1 to 20 of 93

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    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
    nsv4603320copy number variation1nstd183human GRCh37 chr12: 98,317,420-98,339,867 , GRCh38.p12 chr12: 97,923,642-97,946,089 MIR4495
    nsv4426533copy number variation1nstd174human GRCh37 chr12: 98,313,235-98,342,834 , GRCh38.p12 chr12: 97,919,457-97,949,056 MIR4495
    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
    nsv4226928copy number variation1nstd166human GRCh37.p13 chr12: 98,329,763-98,332,674 , GRCh38.p12 chr12: 97,935,985-97,938,896 MIR4495
    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
    nsv3924028copy number variation1nstd102humanUncertain significance NCBI36 chr12: 96,361,122-97,440,614 , GRCh37.p13 chr12: 97,836,991-98,916,483 , GRCh38.p12 chr12: 97,443,213-98,522,705 SLC9A7P1, MIR135A2, 15 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
    nsv3911550copy number variation1nstd102humanLikely pathogenic NCBI36 chr12: 96,312,459-100,328,134 , GRCh37 chr12: 97,788,328-101,804,003 , GRCh38 chr12: 97,394,550-101,410,225 APAF1, ARL1, 45 more genes
    nsv3911099copy number variation1nstd102humanUncertain significance NCBI36 chr12: 96,370,672-97,175,615 , GRCh38 chr12: 97,452,763-98,257,706 , GRCh37 chr12: 97,846,541-98,651,484 MIR4303, RNU6-36P, 5 more genes
    nsv3906006copy number variation1nstd102humanLikely benign GRCh37 chr12: 97,588,490-98,556,589 , GRCh38.p12 chr12: 97,194,712-98,162,811 LOC105369928, PAFAH1B2P2, 10 more genes
    nsv3905447copy number variation2nstd102humanPathogenic GRCh37 chr12: 173,787-133,777,902 , GRCh38.p12 chr12: 64,621-133,201,316 , LOH12CR2, 2452 more genes
    nsv3904719copy number variation1nstd102humanPathogenic GRCh37 chr12: 621,220-133,779,118 , GRCh38.p12 chr12: 512,054-133,202,532 , OR5BT1P, 2441 more genes
    nsv3904242copy number variation1nstd102humanPathogenic GRCh37 chr12: 1-133,851,895 , GRCh38.p12 chr12: 45,740-133,265,309 , RNA5SP369, 2454 more genes
    nsv3900015copy number variation1nstd102humanPathogenic GRCh37 chr12: 94,881,995-103,635,998 , GRCh38.p12 chr12: 94,488,219-103,242,220 CDK17, LOC107984548, 140 more genes
    nsv3897722copy number variation1nstd102humanPathogenic GRCh37 chr12: 191,619-133,777,645 , GRCh38.p12 chr12: 82,453-133,201,059 , RNU4ATAC16P, 2452 more genes
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