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Items: 1 to 20 of 139

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137099copy number variation1nstd102humanPathogenic GRCh37 chr12: 11,463,270-14,019,142 , GRCh38.p12 chr12: 11,310,336-13,866,208 HTR7P1, RPL37AP9, 55 more genes
    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
    nsv7058352inversion1nstd229human GRCh38 chr12: 12,745,693-12,921,544 , GRCh37.p13 chr12: 12,898,627-13,074,478 MIR614, GPRC5A, 7 more genes
    nsv6936930copy number variation1nstd229human GRCh38 chr12: 12,913,354-12,920,286 , GRCh37.p13 chr12: 13,066,288-13,073,220 GPRC5A, MIR614
    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
    nsv6470183copy number variation1nstd223human GRCh38 chr12: 12,756,563-12,941,912 , GRCh37.p13 chr12: 12,909,497-13,094,846 STX8P1, RPL13AP20, 9 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
    nsv6307668insertion1nstd186human GRCh37 chr12: 13,067,527-13,067,530 , GRCh38.p12 chr12: 12,914,593-12,914,596 GPRC5A, MIR614
    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
    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
    nsv6132146copy number variation1nstd213human GRCh37 chr12: 12,970,000-13,590,001 , GRCh38.p12 chr12: 12,817,066-13,437,067 EMP1, GPRC5A, 14 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
    nsv5978020insertion1nstd209human GRCh38 chr12: 12,914,549-12,914,549 , GRCh37.p13 chr12: 13,067,483-13,067,483 GPRC5A, MIR614
    nsv5547965insertion1nstd206human GRCh38 chr12: 12,914,593-12,914,596 , GRCh37.p13 chr12: 13,067,527-13,067,530 GPRC5A, MIR614
    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
    nsv4882300inversion1nstd200human GRCh37 chr12: 6,338,820-22,046,498 , GRCh38.p12 chr12: 6,229,654-21,893,564 , LOC105369686, 414 more genes
    nsv4682144copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr12: 12,869,936-14,135,064 , GRCh38.p12 chr12: 12,717,002-13,982,130 GPR19, EMP1, 26 more genes
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