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Items: 1 to 20 of 160

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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
    nsv7051422inversion1nstd229human GRCh38 chr6: 31,669,217-31,669,311 , GRCh37.p13 chr6: 31,636,994-31,637,088 CSNK2B, LY6G5B
    nsv7045112inversion1nstd229human GRCh38 chr6: 30,561,326-37,907,708 , GRCh37.p13 chr6: 30,529,103-37,875,484 ZBTB22, PNPLA1, 355 more genes
    nsv6413983copy number variation1nstd223human GRCh38 chr6: 31,670,427-31,671,319 , GRCh37.p13 chr6: 31,638,204-31,639,096 LY6G5B, CSNK2B
    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
    nsv6301152copy number variation1nstd186human GRCh37 chr6: 31,638,206-31,639,089 , GRCh38.p12 chr6: 31,670,429-31,671,312 CSNK2B, LY6G5B
    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
    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
    nsv5467263copy number variation1nstd206human GRCh38 chr6: 31,670,429-31,671,312 , GRCh37.p13 chr6: 31,638,206-31,639,089 CSNK2B, LY6G5B
    nsv5362816translocation1nstd200human GRCh38 chr6: 31,670,429-31,670,429 , GRCh38 chr6: 31,671,312-31,671,312 , GRCh37.p13 chr6: 31,638,206-31,638,206 , GRCh37.p13 chr6: 31,639,089-31,639,089 CSNK2B, LY6G5B
    nsv5312460copy number variation1nstd204human GRCh37.p13 chr6: 31,638,201-31,639,098 , GRCh38.p13 chr6: 31,670,424-31,671,321 CSNK2B, LY6G5B
    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
    nsv5229526copy number variation1nstd204human GRCh38.p13 chr6: 31,620,501-31,855,300 , GRCh37.p13 chr6: 31,588,278-31,823,077 LOC105375018, DDAH2, 35 more genes
    nsv4815857copy number variation1nstd200human GRCh37 chr6: 31,638,206-31,639,089 , GRCh38.p12 chr6: 31,670,429-31,671,312 CSNK2B, LY6G5B
    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
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