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Items: 1 to 20 of 101

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6930810copy number variation1nstd229human GRCh38 chr12: 116,465,101-116,547,300 , GRCh37.p13 chr12: 116,902,906-116,985,105 LOC105370007, LINC02457, 2 more genes
    nsv6925773copy number variation1nstd229human GRCh38 chr12: 116,277,201-116,750,600 , GRCh37.p13 chr12: 116,715,006-117,188,405 SPRING1, MIR4472-2, 8 more genes
    nsv6637986copy number variation1nstd102humanUncertain significance GRCh37 chr12: 116,693,045-117,089,243 , GRCh38.p12 chr12: 116,255,240-116,651,438 LOC105370005, LINC00173, 6 more genes
    nsv6637830copy number variation1nstd102humanUncertain significance GRCh37 chr12: 116,422,123-117,740,952 , GRCh38.p12 chr12: 115,984,318-117,303,147 ELOCP32, LOC105370010, 23 more genes
    nsv6621503copy number variation1nstd224human GRCh37 chr12: 116,799,023-117,188,111 , GRCh38.p12 chr12: 116,361,218-116,750,306 SPRING1, RNFT2, 6 more genes
    nsv6314093copy number variation1nstd102humanUncertain significance GRCh37 chr12: 116,869,761-117,330,856 , GRCh38.p12 chr12: 116,431,956-116,893,051 LINC00173, LOC105370008, 8 more genes
    nsv6132320copy number variation1nstd213human GRCh37 chr12: 114,660,000-117,390,001 , GRCh38.p12 chr12: 114,222,195-116,952,196 FBXW8, RPL21P105, 31 more genes
    nsv5928062copy number variation1nstd209human GRCh38 chr12: 116,532,228-116,532,279 , GRCh37.p13 chr12: 116,970,033-116,970,084 LINC00173
    nsv4995804copy number variation1nstd200human GRCh38 chr12: 116,535,323-116,535,399 , GRCh37.p13 chr12: 116,973,128-116,973,204 LINC00173
    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
    nsv4674960copy number variation1nstd102humanUncertain significance GRCh37 chr12: 116,416,809-117,740,952 , GRCh38.p12 chr12: 115,979,004-117,303,147 LINC02457, MAP1LC3B2, 23 more genes
    nsv4456961copy number variation1nstd102humanUncertain significance GRCh37 chr12: 116,551,934-117,093,172 , GRCh38.p12 chr12: 116,114,129-116,655,367 MAP1LC3B2, LOC105370007, 8 more genes
    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
    nsv4223878copy number variation1nstd166human GRCh37.p13 chr12: 116,973,128-116,973,204 , GRCh38.p12 chr12: 116,535,323-116,535,399 LINC00173
    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
    nsv3916921copy number variation1nstd102humanUncertain significance GRCh37 chr12: 116,466,743-117,737,905 , GRCh38 chr12: 116,028,938-117,300,100 , NCBI36 chr12: 114,951,126-116,222,288 LINC00173, FBXW8, 23 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
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