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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5719174mobile element insertion1nstd211human GRCh38 chr4: 181,265,286-181,265,286 , GRCh37.p13 chr4: 182,186,439-182,186,439 LINC02500
    nsv5682184mobile element insertion1nstd211human GRCh38 chr4: 181,265,286-181,265,286 , GRCh37.p13 chr4: 182,186,439-182,186,439 LINC02500
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    nsv5405347mobile element insertion1nstd206human GRCh38 chr4: 181,265,286-181,265,310 , GRCh37.p13 chr4: 182,186,439-182,186,463 LINC02500
    nsv5302159copy number variation1nstd204human GRCh38.p13 chr4: 181,036,776-181,262,708 , GRCh37.p13 chr4: 181,957,929-182,183,861 LINC02500, LINC00290
    nsv5240008copy number variation1nstd204human GRCh38.p13 chr4: 181,242,768-181,261,850 , GRCh37.p13 chr4: 182,163,921-182,183,003 LINC02500
    nsv5233477copy number variation1nstd204human GRCh38.p13 chr4: 181,257,601-181,263,600 , GRCh37.p13 chr4: 182,178,754-182,184,753 LINC02500
    nsv5200366copy number variation1nstd102humanLikely pathogenic GRCh37 chr4: 179,554,876-190,916,678 , GRCh38.p12 chr4: 178,633,722-189,995,523 SLC25A4, CASP3, 151 more genes
    nsv4930335copy number variation1nstd200human GRCh38 chr4: 181,263,428-181,264,856 , GRCh37.p13 chr4: 182,184,581-182,186,009 LINC02500
    nsv4930334copy number variation1nstd200human GRCh38 chr4: 181,261,417-181,265,585 , GRCh37.p13 chr4: 182,182,570-182,186,738 LINC02500
    nsv4801985copy number variation1nstd200human GRCh37 chr4: 182,184,581-182,186,009 , GRCh38.p12 chr4: 181,263,428-181,264,856 LINC02500
    nsv4801984copy number variation1nstd200human GRCh37 chr4: 182,182,570-182,186,738 , GRCh38.p12 chr4: 181,261,417-181,265,585 LINC02500
    nsv4761770inversion1nstd199human GRCh37 chr4: 34,988-191,015,248 , GRCh38.p12 chr4: 34,988-190,094,093 , ADD1, 2433 more genes
    nsv4758212inversion1nstd199human GRCh37 chr4: 30,775-191,019,445 , GRCh38.p12 chr4: 30,775-190,098,290 , ADD1, 2433 more genes
    nsv4754592inversion1nstd199human GRCh37 chr4: 27,111-191,020,337 , GRCh38.p12 chr4: 27,111-190,099,182 , ADD1, 2433 more genes
    nsv4753570inversion1nstd199human GRCh37 chr4: 19,034-191,028,414 , GRCh38.p12 chr4: 19,034-190,107,259 , ADD1, 2434 more genes
    nsv4751554inversion1nstd199human GRCh37 chr4: 18,939-191,034,785 , GRCh38.p12 chr4: 18,939-190,113,630 , ADD1, 2434 more genes
    nsv4729375copy number variation1nstd102humanPathogenic GRCh37 chr4: 169,108,358-184,425,536 , GRCh38.p12 chr4: 168,187,207-183,504,383 GALNT7-DT, LOC105377524, 154 more genes
    nsv4728923copy number variation1nstd102humanUncertain significance GRCh37 chr4: 181,853,722-184,723,116 , GRCh38.p12 chr4: 180,932,569-183,801,963 RNU6-479P, LOC105377581, 41 more genes
    nsv4674658copy number variation1nstd102humanPathogenic GRCh37 chr4: 178,566,256-190,957,473 , GRCh38.p12 chr4: 177,645,102-190,036,318 RARRES2P4, ING2-DT, 165 more genes
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