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Items: 1 to 20 of 180

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137328insertion1nstd232human GRCh37.p13 chr12: 10,852,255-10,852,255 , GRCh38.p12 chr12: 10,699,656-10,699,656 YBX3
    nsv7098813copy number variation1nstd102humanPathogenic GRCh37 chr12: 176,047-34,179,852 , GRCh38.p12 chr12: 66,881-34,026,917 TDGP1, RPS4XP14, 680 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
    nsv7064789inversion1nstd229human GRCh38 chr12: 10,249,571-12,880,432 , GRCh37.p13 chr12: 10,402,170-13,033,366 DDX47, TAS2R64P, 89 more genes
    nsv7064629inversion1nstd229human GRCh38 chr12: 10,296,462-11,054,955 , GRCh37.p13 chr12: 10,449,061-11,207,554 TAS2R31, EIF2S3B, 39 more genes
    nsv7061545inversion1nstd229human GRCh38 chr12: 10,483,551-11,289,523 , GRCh37.p13 chr12: 10,636,150-11,442,457 TAS2R14, EIF2S3B, 40 more genes
    nsv6931101copy number variation1nstd229human GRCh38 chr12: 10,720,422-10,881,002 , GRCh37.p13 chr12: 10,873,021-11,033,601 PRR4, HSPE1P12, 10 more genes
    nsv6923241copy number variation1nstd229human GRCh38 chr12: 10,700,801-10,707,300 , GRCh37.p13 chr12: 10,853,400-10,859,899 YBX3
    nsv6919750copy number variation1nstd229human GRCh38 chr12: 10,713,332-10,715,692 , GRCh37.p13 chr12: 10,865,931-10,868,291 YBX3
    nsv6918499copy number variation1nstd229human GRCh38 chr12: 10,710,753-10,716,364 , GRCh37.p13 chr12: 10,863,352-10,868,963 YBX3
    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
    nsv6577070inversion1nstd223human GRCh38 chr12: 10,714,799-10,715,507 , GRCh37.p13 chr12: 10,867,398-10,868,106 YBX3
    nsv6465372copy number variation1nstd223human GRCh38 chr12: 10,720,422-10,881,002 , GRCh37.p13 chr12: 10,873,021-11,033,601 PRR4, HSPE1P12, 10 more genes
    nsv6304923copy number variation1nstd186human GRCh37 chr12: 10,853,416-10,853,836 , GRCh38.p12 chr12: 10,700,817-10,701,237 YBX3
    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
    nsv6132616copy number variation1nstd213human GRCh37 chr12: 8,100,000-12,900,001 , GRCh38.p12 chr12: 7,947,404-12,747,067 A2M, A2MP1, 178 more genes
    nsv6132445copy number variation1nstd213human GRCh37 chr12: 9,040,000-11,190,001 , GRCh38.p12 chr12: 8,887,404-11,037,402 A2M, A2MP1, 95 more genes
    nsv6132422copy number variation1nstd213human GRCh37 chr12: 190,000-30,830,001 , GRCh38.p12 chr12: 80,834-30,677,067 , A2M, 622 more genes
    nsv6132212copy number variation1nstd213human GRCh37 chr12: 10,670,000-12,390,001 , GRCh38.p12 chr12: 10,517,401-12,237,067 ETV6, LRP6, 57 more genes
    nsv6132133copy number variation1nstd213human GRCh37 chr12: 10,400,000-11,220,001 , GRCh38.p12 chr12: 10,247,401-11,067,402 KLRC2, PRH1, 41 more genes
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