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Items: 1 to 20 of 140

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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
    nsv7064011inversion1nstd229human GRCh38 chr12: 11,255,910-17,864,916 , GRCh37.p13 chr12: 11,408,826-18,017,850 MGP, MIR3974, 108 more genes
    nsv6634456copy number variation1nstd102humanPathogenic GRCh37 chr12: 10,853,887-24,103,810 , GRCh38.p12 chr12: 10,701,288-23,950,876 TAS2R15P, LOC105369673, 209 more genes
    nsv6309465copy number variation2nstd102humanUncertain significance GRCh37 chr12: 11,803,062-15,835,885 , GRCh38.p12 chr12: 11,650,128-15,682,951 LRP6, APOLD1, 78 more genes
    nsv6309308copy number variation1nstd102humanUncertain significance GRCh37 chr12: 14,849,146-15,669,910 , GRCh38.p12 chr12: 14,696,212-15,516,976 PTPRO, RERG, 17 more genes
    nsv6132720copy number variation1nstd213human GRCh37 chr12: 9,040,000-17,930,001 , GRCh38.p12 chr12: 8,887,404-17,777,067 A2M, A2MP1, 215 more genes
    nsv6132422copy number variation1nstd213human GRCh37 chr12: 190,000-30,830,001 , GRCh38.p12 chr12: 80,834-30,677,067 , A2M, 622 more genes
    nsv6132418copy number variation1nstd213human GRCh37 chr12: 14,930,000-15,180,001 , GRCh38.p12 chr12: 14,777,066-15,027,067 ARHGDIB, ART4, 8 more genes
    nsv6132416copy number variation1nstd213human GRCh37 chr12: 13,780,000-20,840,001 , GRCh38.p12 chr12: 13,627,066-20,687,067 ARHGDIB, ART4, 87 more genes
    nsv6132215copy number variation1nstd213human GRCh37 chr12: 11,360,000-16,150,001 , GRCh38.p12 chr12: 11,207,094-15,997,067 ARHGDIB, ART4, 93 more genes
    nsv6132138copy number variation1nstd213human GRCh37 chr12: 11,250,000-19,950,001 , GRCh38.p12 chr12: 11,097,401-19,797,067 ARHGDIB, ART4, 139 more genes
    nsv5323122inversion1nstd204human GRCh37.p13 chr12: 6,338,815-22,046,498 , GRCh38.p13 chr12: 6,229,649-21,893,564 , A2M, 414 more genes
    nsv5029743inversion1nstd200human GRCh38 chr12: 7,297,013-15,308,349 , GRCh37.p13 chr12: 7,449,609-15,461,283 , MIR1244-4, 259 more genes
    nsv4981286copy number variation1nstd200human GRCh38 chr12: 14,814,456-14,816,902 , GRCh37.p13 chr12: 14,967,390-14,969,836 C12orf60, SMCO3
    nsv4882300inversion1nstd200human GRCh37 chr12: 6,338,820-22,046,498 , GRCh38.p12 chr12: 6,229,654-21,893,564 , LOC105369686, 414 more genes
    nsv4837641copy number variation1nstd200human GRCh37 chr12: 14,967,390-14,969,836 , GRCh38.p12 chr12: 14,814,456-14,816,902 SMCO3, C12orf60
    nsv4675174copy number variation1nstd102humanPathogenic GRCh37 chr12: 11,737,824-16,780,886 , GRCh38.p12 chr12: 11,584,890-16,627,952 LOC107001063, RN7SKP162, 89 more genes
    nsv4674941copy number variation1nstd102humanPathogenic GRCh37 chr12: 274,676-37,869,301 , GRCh38.p12 chr12: 165,510-37,475,499 LOC105376675, ATF7IP, 682 more genes
    nsv4455458copy number variation1nstd102humanPathogenic GRCh37 chr12: 173,786-34,496,628 , GRCh38.p12 chr12: 64,620-34,343,693 EMP1, PLBD1-AS1, 684 more genes
    nsv4436483complex substitution1nstd102humanassociation NCBI36 chr12: 13,090,968-16,310,672 , GRCh38.p12 chr12: 13,046,767-16,266,471 , GRCh37.p13 chr12: 13,199,701-16,419,405 ARHGDIB, ART4, 48 more genes
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