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Items: 1 to 20 of 165

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112738copy number variation1nstd102humanPathogenic GRCh37 chr6: 149,619-3,951,208 , GRCh38.p12 chr6: 149,619-3,950,974 LINC01600, TUBB2BP1, 66 more genes
    nsv5897284copy number variation1nstd209human GRCh38 chr6: 3,720,330-3,720,608 , GRCh37.p13 chr6: 3,720,564-3,720,842 PXDC1, LOC100507336
    nsv5637231insertion1nstd207human GRCh38 chr6: 3,721,956-3,721,956 , GRCh37.p13 chr6: 3,722,190-3,722,190 PXDC1
    nsv5097358mobile element insertion1nstd203human GRCh38 chr6: 3,741,414-3,741,424 , GRCh37.p13 chr6: 3,741,648-3,741,658 PXDC1
    nsv4947468copy number variation1nstd200human GRCh38 chr6: 3,733,696-3,739,682 , GRCh37.p13 chr6: 3,733,930-3,739,916 PXDC1
    nsv4809485copy number variation1nstd200human GRCh37 chr6: 3,733,930-3,739,916 , GRCh38.p12 chr6: 3,733,696-3,739,682 PXDC1
    nsv4675171copy number variation1nstd102humanUncertain significance GRCh37 chr6: 3,409,111-3,734,008 , GRCh38.p12 chr6: 3,408,877-3,733,774 LOC643327, PXDC1, 4 more genes
    nsv4492585mobile element insertion1nstd166human GRCh37.p13 chr6: 3,741,648-3,741,648 , GRCh38.p12 chr6: 3,741,414-3,741,414 PXDC1
    nsv4456780copy number variation1nstd102humanPathogenic GRCh37 chr6: 156,974-23,221,621 , GRCh38.p12 chr6: 156,974-23,221,393 LOC105374960, LOC101928573, 342 more genes
    nsv4129780copy number variation1nstd166human GRCh37.p13 chr6: 3,733,344-3,733,489 , GRCh38.p12 chr6: 3,733,110-3,733,255 PXDC1
    nsv4120528copy number variation1nstd166human GRCh37.p13 chr6: 3,733,930-3,739,916 , GRCh38.p12 chr6: 3,733,696-3,739,682 PXDC1
    nsv4119355copy number variation1nstd166human GRCh37.p13 chr6: 3,732,759-3,744,128 , GRCh38.p12 chr6: 3,732,525-3,743,894 PXDC1
    nsv3923249copy number variation1nstd102humanPathogenic NCBI36 chr6: 110,675-8,981,266 , GRCh38 chr6: 165,675-9,036,034 , GRCh37 chr6: 165,675-9,036,267 LOC100506207, LOC105374889, 148 more genes
    nsv3922576copy number variation1nstd102humanPathogenic GRCh37 chr6: 164,633-6,284,470 , GRCh38 chr6: 164,633-6,284,237 , NCBI36 chr6: 109,633-6,229,469 GLRX3P2, CDYL, 106 more genes
    nsv3922052copy number variation1nstd102humanPathogenic GRCh37 chr6: 155,807-17,058,645 , NCBI36 chr6: 100,807-17,166,624 , GRCh38 chr6: 155,807-17,058,414 ECI2-DT, RNU1-11P, 268 more genes
    nsv3921817copy number variation1nstd102humanPathogenic GRCh37 chr6: 2,862,874-16,698,019 , GRCh38 chr6: 2,862,640-16,697,788 , NCBI36 chr6: 2,807,873-16,805,998 RN7SKP293, LOC105374906, 230 more genes
    nsv3921201copy number variation1nstd102humanUncertain significance NCBI36 chr6: 101,974-4,892,090 , GRCh37 chr6: 156,974-4,947,091 , GRCh38 chr6: 156,974-4,946,857 LOC100422781, RN7SL352P, 86 more genes
    nsv3921027copy number variation1nstd102humanPathogenic GRCh38 chr6: 389,423-13,474,956 , GRCh37 chr6: 389,423-13,475,188 , NCBI36 chr6: 334,423-13,583,167 LOC105374898, HIVEP1, 215 more genes
    nsv3920564copy number variation1nstd102humanPathogenic GRCh38 chr6: 3,224,310-30,657,190 , GRCh37 chr6: 3,224,544-30,624,967 , NCBI36 chr6: 3,169,543-30,732,946 PRELID1P2, RPL7AP7, 785 more genes
    nsv3920236copy number variation1nstd102humanPathogenic GRCh37 chr6: 164,633-5,823,834 , GRCh38 chr6: 164,633-5,823,601 , NCBI36 chr6: 109,633-5,768,833 TUBB2A, SERPINB9-AS1, 98 more genes
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