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Items: 1 to 20 of 168

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7142235copy number variation1nstd232human GRCh37.p13 chr6: 31,827,721-31,827,816 , GRCh38.p12 chr6: 31,859,944-31,860,039 NEU1
    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
    nsv6794938copy number variation1nstd229human GRCh38 chr6: 31,856,908-31,862,360 , GRCh37.p13 chr6: 31,824,685-31,830,137 NEU1, SLC44A4
    nsv6794416copy number variation1nstd229human GRCh38 chr6: 31,852,229-31,890,598 , GRCh37.p13 chr6: 31,820,006-31,858,375 EHMT2, SLC44A4, 2 more genes
    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
    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
    nsv6140608copy number variation1nstd206human GRCh38 chr6: 31,752,000-31,862,000 , GRCh37.p13 chr6: 31,719,777-31,829,777 LSM2, SLC44A4, 14 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
    nsv5980377copy number variation1nstd102humanUncertain significance GRCh37 chr6: 31,827,495-31,830,553 , GRCh38.p12 chr6: 31,859,718-31,862,776 NEU1, SLC44A4
    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
    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
    nsv4683984copy number variation1nstd102humanPathogenic GRCh37 chr6: 31,824,828-31,834,398 , GRCh38.p12 chr6: 31,857,051-31,866,621 SLC44A4, NEU1
    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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