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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
    nsv5689018mobile element insertion2nstd211human GRCh38 chr6: 2,638,439-2,638,439 , GRCh37.p13 chr6: 2,638,673-2,638,673 LINC02521
    nsv5460709copy number variation1nstd206human GRCh38 chr6: 2,093,576-2,775,922 , GRCh37.p13 chr6: 2,093,810-2,776,156 GMDS, WRNIP1, 6 more genes
    nsv5398339mobile element insertion1nstd206human GRCh38 chr6: 2,638,439-2,638,490 , GRCh37.p13 chr6: 2,638,673-2,638,724 LINC02521
    nsv4940385copy number variation1nstd200human GRCh38 chr6: 2,627,864-2,633,188 , GRCh37.p13 chr6: 2,628,098-2,633,422 LINC02521, LINC01600
    nsv4809458copy number variation1nstd200human GRCh37 chr6: 2,628,098-2,633,422 , GRCh38.p12 chr6: 2,627,864-2,633,188 LINC02521, LINC01600
    nsv4729315copy number variation1nstd102humanPathogenic GRCh37 chr6: 302,183-3,290,583 , GRCh38.p12 chr6: 302,183-3,290,349 RIPK1, MARK2P18, 53 more genes
    nsv4675890copy number variation1nstd102humanUncertain significance GRCh37 chr6: 2,167,407-2,775,133 , GRCh38.p12 chr6: 2,167,173-2,774,899 LINC02521, LOC107986512, 6 more genes
    nsv4456780copy number variation1nstd102humanPathogenic GRCh37 chr6: 156,974-23,221,621 , GRCh38.p12 chr6: 156,974-23,221,393 LOC105374960, LOC101928573, 342 more genes
    nsv3923261copy number variation1nstd102humanPathogenic NCBI36 chr6: 1,415,511-2,642,839 , GRCh37.p13 chr6: 1,470,512-2,697,840 , GRCh38.p12 chr6: 1,470,277-2,697,606 FOXC1, HMGN2P28, 13 more genes
    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
    nsv3923206copy number variation1nstd102humanPathogenic NCBI36 chr6: 108,083-3,404,840 , GRCh38 chr6: 163,083-3,459,607 , GRCh37 chr6: 163,083-3,459,841 LOC105374883, MIR4645, 58 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
    nsv3921409copy number variation1nstd102humanUncertain significance NCBI36 chr6: 1,435,871-2,622,722 , GRCh37 chr6: 1,490,872-2,677,723 , GRCh38 chr6: 1,490,637-2,677,489 LINC02521, LOC107986555, 13 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
    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
    nsv3918808copy number variation1nstd102humanPathogenic NCBI36 chr6: 1,435,870-2,645,239 , GRCh38 chr6: 1,490,636-2,700,006 , GRCh37 chr6: 1,490,871-2,700,240 MYLK4, FOXCUT, 13 more genes
    nsv3918645copy number variation1nstd102humanLikely pathogenic NCBI36 chr6: 101,974-11,659,036 , GRCh37 chr6: 156,974-11,551,050 , GRCh38 chr6: 156,974-11,550,817 BMP6, BPHL, 194 more genes
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