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Items: 1 to 20 of 106

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5973346inversion1nstd209human GRCh38 chr12: 118,054,601-123,705,841 , GRCh37.p13 chr12: 118,492,406-124,190,388 , ACADS, 162 more genes
    nsv5506917copy number variation1nstd206human GRCh38 chr12: 118,137,755-118,141,140 , GRCh37.p13 chr12: 118,575,560-118,578,945 PEBP1
    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
    nsv4680133copy number variation1nstd189human GRCh37.p13 chr12: 118,431,926-118,855,845 , GRCh38.p12 chr12: 117,994,121-118,418,040 PEBP1, RFC5, 6 more genes
    nsv4675388copy number variation1nstd102humanUncertain significance GRCh37 chr12: 117,858,408-118,668,114 , GRCh38.p12 chr12: 117,420,603-118,230,309 LOC101928274, LOC105370012, 7 more genes
    nsv4617178copy number variation1nstd183human GRCh37 chr12: 118,561,298-118,584,117 , GRCh38.p12 chr12: 118,123,493-118,146,312 PEBP1, LOC101928274
    nsv4455668copy number variation1nstd102humanUncertain significance GRCh37 chr12: 116,718,607-119,728,623 , GRCh38.p12 chr12: 116,280,802-119,290,818 LINC00934, LOC105370019, 53 more genes
    nsv3924220copy number variation1nstd102humanPathogenic GRCh38 chr12: 115,131,583-133,166,920 , NCBI36 chr12: 114,053,771-132,253,579 , GRCh37 chr12: 115,569,388-133,743,506 LOC105370080, LINC02985, 376 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
    nsv3913894copy number variation1nstd102humanPathogenic NCBI36 chr12: 113,190,591-132,287,975 , GRCh38 chr12: 114,268,403-133,201,316 , GRCh37 chr12: 114,706,208-133,777,902 TAOK3, LINC02405, 386 more genes
    nsv3906446copy number variation1nstd102humanLikely pathogenic GRCh37 chr12: 118,486,842-120,995,382 , GRCh38.p12 chr12: 118,049,037-120,557,579 COX6A1, MSI1, 63 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
    nsv3898723copy number variation1nstd102humanUncertain significance GRCh37 chr12: 118,258,061-118,726,805 , GRCh38.p12 chr12: 117,820,256-118,289,000 LOC101928274, PEBP1, 7 more genes
    nsv3898298copy number variation1nstd102humanPathogenic GRCh37 chr12: 116,028,864-118,791,808 , GRCh38.p12 chr12: 115,591,059-118,354,003 LOC101928274, MIR4472-2, 38 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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