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Items: 1 to 20 of 171

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098813copy number variation1nstd102humanPathogenic GRCh37 chr12: 176,047-34,179,852 , GRCh38.p12 chr12: 66,881-34,026,917 TDGP1, RPS4XP14, 680 more genes
    nsv7094047copy number variation1nstd102humanUncertain significance GRCh37 chr12: 4,368,352-9,027,607 , GRCh38.p12 chr12: 4,259,186-8,875,011 ACRBP, OR7E148P, 165 more genes
    nsv7074628inversion1nstd229human GRCh38 chr12: 5,173,229-8,663,348 , GRCh37.p13 chr12: 5,282,395-8,815,944 P3H3, LOC105369621, 141 more genes
    nsv7072221inversion1nstd229human GRCh38 chr12: 4,055,290-11,695,188 , GRCh37.p13 chr12: 4,164,456-11,848,122 RN7SL69P, KLRA1P, 285 more genes
    nsv6937285copy number variation1nstd229human GRCh38 chr12: 6,317,901-6,334,500 , GRCh37.p13 chr12: 6,427,067-6,443,666 TNFRSF1A, PLEKHG6
    nsv6937180copy number variation1nstd229human GRCh38 chr12: 6,342,401-6,356,600 , GRCh37.p13 chr12: 6,451,567-6,465,766 RN7SL391P, LOC112268088, 3 more genes
    nsv6930965copy number variation1nstd229human GRCh38 chr12: 4,486,494-6,353,198 , GRCh37.p13 chr12: 4,595,660-6,462,364 LOC112268088, NTF3, 34 more genes
    nsv6922286copy number variation1nstd229human GRCh38 chr12: 6,158,793-6,527,112 , GRCh37.p13 chr12: 6,267,959-6,636,278 SCARNA10, PKP2P1, 21 more genes
    nsv6918804copy number variation1nstd229human GRCh38 chr12: 6,331,401-6,335,600 , GRCh37.p13 chr12: 6,440,567-6,444,766 TNFRSF1A
    nsv6637376copy number variation1nstd102humanPathogenic GRCh37 chr12: 173,787-8,320,544 , GRCh38.p12 chr12: 64,621-8,167,948 GCSHP4, RNU7-1, 220 more genes
    nsv6472373copy number variation1nstd223human GRCh38 chr12: 6,012,501-7,083,600 , GRCh37.p13 chr12: 6,121,667-7,189,876 GPR162, CD27, 71 more genes
    nsv6472196copy number variation1nstd223human GRCh38 chr12: 6,013,501-7,083,700 , GRCh37.p13 chr12: 6,122,667-7,189,876 SCARNA10, ATP5MFP5, 71 more genes
    nsv6309483copy number variation1nstd102humanUncertain significance GRCh37 chr12: 6,438,478-8,756,953 , GRCh38.p12 chr12: 6,329,312-8,604,357 ENPP7P5, GPR162, 122 more genes
    nsv6309326copy number variation2nstd102humanUncertain significance GRCh37 chr12: 6,438,478-8,248,686 , GRCh38.p12 chr12: 6,329,312-8,096,090 NANOGNB, SCNN1A, 94 more genes
    nsv6290722copy number variation1nstd102humanUncertain significance GRCh37 chr12: 6,407,226-6,491,280 , GRCh38.p12 chr12: 6,298,060-6,382,114 TNFRSF1A, LTBR, 6 more genes
    nsv6290254copy number variation1nstd102humanPathogenic GRCh37 chr12: 146,240-8,330,229 , GRCh38.p12 chr12: 45,740-8,177,633 CLEC4A, FBXL14, 220 more genes
    nsv6132430copy number variation1nstd213human GRCh37 chr12: 6,290,000-6,680,001 , GRCh38.p12 chr12: 6,180,834-6,570,835 CD9, CHD4, 25 more genes
    nsv6132422copy number variation1nstd213human GRCh37 chr12: 190,000-30,830,001 , GRCh38.p12 chr12: 80,834-30,677,067 , A2M, 622 more genes
    nsv6112763copy number variation1nstd102humanPathogenic GRCh37 chr12: 189,145-7,730,395 , GRCh38.p12 chr12: 79,979-7,577,799 GALNT8, LINC02371, 197 more genes
    nsv5564211copy number variation1nstd102humanUncertain significance GRCh37 chr12: 6,438,478-7,362,819 , GRCh38.p12 chr12: 6,329,312-7,210,223 GPR162, SCARNA11, 68 more genes
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