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Items: 1 to 20 of 141

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7051940inversion1nstd229human GRCh38 chr6: 28,627,967-29,067,478 , GRCh37.p13 chr6: 28,595,744-29,035,255 ZNF90P2, TRK-TTT13-1, 51 more genes
    nsv6797813copy number variation1nstd229human GRCh38 chr6: 28,799,001-29,042,500 , GRCh37.p13 chr6: 28,766,778-29,010,277 TRR-CCG1-2, ZNF311, 28 more genes
    nsv6796844copy number variation1nstd229human GRCh38 chr6: 28,888,801-28,898,900 , GRCh37.p13 chr6: 28,856,578-28,866,677 HCG14, ZNF90P2, 1 more genes
    nsv6564524inversion1nstd223human GRCh38 chr6: 28,831,504-29,349,940 , GRCh37.p13 chr6: 28,799,281-29,317,717 OR2U2P, TRL-AAG3-1, 44 more genes
    nsv6563406inversion1nstd223human GRCh38 chr6: 25,888,425-29,704,317 , GRCh37.p13 chr6: 25,888,653-29,672,094 OR1F12P, H4C2, 362 more genes
    nsv6408266copy number variation1nstd223human GRCh38 chr6: 28,882,481-28,920,690 , GRCh37.p13 chr6: 28,850,258-28,888,467 HCG14, RNU6-930P, 3 more genes
    nsv6302467copy number variation1nstd186human GRCh37 chr6: 28,850,258-28,888,468 , GRCh38.p12 chr6: 28,882,481-28,920,691 TRIM27, HCG14, 3 more genes
    nsv6289880copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 28,005,012-31,683,185 , GRCh38.p12 chr6: 28,037,234-31,715,408 ABCF1, AIF1, 313 more genes
    nsv6135508copy number variation1nstd213human GRCh37 chr6: 27,710,000-30,110,001 , GRCh38.p12 chr6: 27,742,221-30,142,224 GABBR1, H1-5, 224 more genes
    nsv5968268inversion1nstd209human GRCh38 chr6: 28,831,490-29,349,953 , GRCh37.p13 chr6: 28,799,267-29,317,730 KRT18P1, TRIM27, 44 more genes
    nsv5472184copy number variation1nstd206human GRCh38 chr6: 28,889,797-28,896,328 , GRCh37.p13 chr6: 28,857,574-28,864,105 ZNF90P2, TRL-CAA1-1, 1 more genes
    nsv5462544copy number variation1nstd206human GRCh38 chr6: 28,882,481-28,920,691 , GRCh37.p13 chr6: 28,850,258-28,888,468 HCG14, RNU6-930P, 3 more genes
    nsv5455264copy number variation1nstd206human GRCh38 chr6: 28,895,901-28,896,244 , GRCh37.p13 chr6: 28,863,678-28,864,021 TRL-CAA1-1, HCG14
    nsv5366813translocation1nstd200human GRCh38 chr1: 37,967,138-37,967,138 , GRCh38 chr6: 28,896,127-28,896,127 , GRCh37.p13 chr1: 38,432,810-38,432,810 , GRCh37.p13 chr6: 28,863,904-28,863,904 SF3A3, HCG14, 1 more genes
    nsv5366809translocation1nstd200human GRCh38 chr1: 37,966,765-37,966,765 , GRCh38 chr6: 28,895,823-28,895,823 , GRCh37.p13 chr1: 38,432,437-38,432,437 , GRCh37.p13 chr6: 28,863,600-28,863,600 SF3A3, HCG14, 1 more genes
    nsv5339495translocation1nstd200human GRCh37 chr1: 38,432,765-38,432,765 , GRCh37 chr6: 28,863,598-28,863,598 , GRCh38.p12 chr1: 37,967,093-37,967,093 , GRCh38.p12 chr6: 28,895,821-28,895,821 SF3A3, HCG14, 1 more genes
    nsv5329462translocation1nstd204human GRCh38.p13 chr6: 28,895,821-28,895,821 , GRCh37.p13 chr6: 28,863,598-28,863,598 , GRCh38.p13 chr1: 37,967,093-37,967,093 , GRCh37.p13 chr1: 38,432,765-38,432,765 SF3A3, HCG14, 1 more genes
    nsv5119910mobile element insertion1nstd203human GRCh38 chr6: 28,896,122-28,896,169 , GRCh37.p13 chr6: 28,863,899-28,863,946 TRL-CAA1-1, HCG14
    nsv5117878mobile element insertion1nstd203human GRCh38 chr6: 28,896,100-28,896,122 , GRCh37.p13 chr6: 28,863,877-28,863,899 TRL-CAA1-1, HCG14
    nsv5117306mobile element insertion1nstd203human GRCh38 chr6: 28,896,077-28,896,121 , GRCh37.p13 chr6: 28,863,854-28,863,898 TRL-CAA1-1, HCG14
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