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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7073020inversion1nstd229human GRCh38 chr12: 96,481,691-98,593,227 , GRCh37.p13 chr12: 96,875,469-98,987,005 TRW-CCA4-1, LINC02409, 26 more genes
    nsv7064866inversion1nstd229human GRCh38 chr12: 97,421,900-98,025,255 , GRCh37.p13 chr12: 97,815,678-98,419,033 MIR135A2, RMST, 5 more genes
    nsv6922635copy number variation1nstd229human GRCh38 chr12: 96,115,345-104,800,221 , GRCh37.p13 chr12: 96,509,123-105,193,999 RNY1P16, CHST11, 121 more genes
    nsv6622098copy number variation1nstd224human GRCh37 chr12: 96,914,613-97,927,063 , GRCh38.p12 chr12: 96,520,835-97,533,285 RMST, LOC105369928, 9 more genes
    nsv6143026copy number variation1nstd206human GRCh38 chr12: 48,500,915-111,724,058 , GRCh37.p13 chr12: 48,894,698-112,161,862 , LINC00592, 1206 more genes
    nsv6132521copy number variation1nstd213human GRCh37 chr12: 97,760,000-100,480,001 , GRCh38.p12 chr12: 97,366,222-100,086,223 TMPO, ANKS1B, 26 more genes
    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
    nsv4384313copy number variation1nstd173human GRCh37 chr12: 97,870,508-97,900,212 , GRCh38.p12 chr12: 97,476,730-97,506,434 RMST, MIR1251
    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
    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
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