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Items: 1 to 20 of 188

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097426copy number variation1nstd102humanUncertain significance GRCh37 chr6: 30,695,893-36,953,949 , GRCh38.p12 chr6: 30,728,116-36,986,173 LEMD2, PSORS1C1, 321 more genes
    nsv7097325copy number variation1nstd102humanUncertain significance GRCh37 chr6: 30,695,893-31,937,492 , GRCh38.p12 chr6: 30,728,116-31,969,715 HCG21, SNORD84, 117 more genes
    nsv7053830inversion1nstd229human GRCh38 chr6: 29,164,448-38,692,657 , GRCh37.p13 chr6: 29,132,225-38,660,433 GTF2H4, RNF8, 472 more genes
    nsv7045112inversion1nstd229human GRCh38 chr6: 30,561,326-37,907,708 , GRCh37.p13 chr6: 30,529,103-37,875,484 ZBTB22, PNPLA1, 355 more genes
    nsv6791203copy number variation1nstd229human GRCh38 chr6: 31,901,801-31,911,000 , GRCh37.p13 chr6: 31,869,578-31,878,777 C2, ZBTB12
    nsv6783395copy number variation1nstd229human GRCh38 chr6: 31,902,401-31,911,000 , GRCh37.p13 chr6: 31,870,178-31,878,777 ZBTB12, C2
    nsv6779807copy number variation1nstd229human GRCh38 chr6: 31,800,134-32,311,768 , GRCh37.p13 chr6: 31,767,911-32,279,545 NELFE, CYP21A1P, 43 more genes
    nsv6412366copy number variation1nstd223human GRCh38 chr6: 31,901,401-31,910,900 , GRCh37.p13 chr6: 31,869,178-31,878,677 C2, ZBTB12
    nsv6402266copy number variation1nstd223human GRCh38 chr6: 31,522,086-32,653,908 , GRCh37.p13 chr6: 31,489,863-32,621,685 MIR6833, LY6G5B, 102 more genes
    nsv6135917copy number variation1nstd213human GRCh37 chr6: 30,110,000-32,450,001 , GRCh38.p12 chr6: 30,142,223-32,482,224 ABCF1, AGER, 186 more genes
    nsv6078300insertion1nstd212human GRCh38 chr6: 31,899,654-31,899,654 , GRCh37.p13 chr6: 31,867,431-31,867,431 C2, ZBTB12
    nsv5235615copy number variation1nstd204human GRCh38.p13 chr6: 31,902,701-32,045,200 , GRCh37.p13 chr6: 31,870,478-32,012,977 STK19, ZBTB12, 14 more genes
    nsv5234405copy number variation1nstd204human GRCh38.p13 chr6: 30,240,001-32,313,700 , GRCh37.p13 chr6: 30,207,778-32,281,477 DDAH2, LOC105375018, 175 more genes
    nsv5229879copy number variation1nstd204human GRCh38.p13 chr6: 31,502,001-32,151,900 , GRCh37.p13 chr6: 31,469,778-32,119,677 LTB, PPT2, 80 more genes
    nsv5188852mobile element insertion1nstd203human GRCh38 chr6: 31,898,215-31,898,228 , GRCh37.p13 chr6: 31,865,992-31,866,005 C2, ZBTB12
    nsv4757608inversion1nstd199human GRCh37 chr6: 26,743,921-58,149,359 , GRCh38.p12 chr6: 26,823,536-61,119,912 , ABCF1, 1075 more genes
    nsv4756329inversion1nstd199human GRCh37 chr6: 26,745,246-58,149,317 , GRCh38.p12 chr6: 26,823,536-61,119,912 , ABCF1, 1075 more genes
    nsv4735754copy number variation1nstd199human GRCh37 chr6: 26,776,020-58,144,810 , GRCh38.p12 chr6: 26,823,536-61,119,912 , RNU6-250P, 1075 more genes
    nsv4707238copy number variation1nstd195human GRCh38.p12 chr6: 31,855,324-31,931,374 , GRCh37 chr6: 31,823,101-31,899,151 C2, NEU1, 4 more genes
    nsv4675941copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 31,036,397-34,088,832 , GRCh38.p12 chr6: 31,068,620-34,121,055 AGER, AIF1, 217 more genes
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