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Items: 1 to 20 of 144

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7140329copy number variation1nstd232human GRCh37.p13 chr6: 30,515,049-30,515,125 , GRCh38.p12 chr6: 30,547,272-30,547,348 GNL1
    nsv7053830inversion1nstd229human GRCh38 chr6: 29,164,448-38,692,657 , GRCh37.p13 chr6: 29,132,225-38,660,433 GTF2H4, RNF8, 472 more genes
    nsv7045629inversion1nstd229human GRCh38 chr6: 30,007,594-31,355,527 , GRCh37.p13 chr6: 29,975,371-31,323,304 USP8P1, LINC02571, 82 more genes
    nsv6795673copy number variation1nstd229human GRCh38 chr6: 30,444,101-31,201,100 , GRCh37.p13 chr6: 30,411,878-31,168,877 POU5F1, DDR1, 51 more genes
    nsv6794247copy number variation1nstd229human GRCh38 chr6: 30,380,601-31,245,000 , GRCh37.p13 chr6: 30,348,378-31,212,777 MUC22, TMPOP1, 52 more genes
    nsv6778547copy number variation1nstd229human GRCh38 chr6: 30,544,069-30,545,233 , GRCh37.p13 chr6: 30,511,846-30,513,010 GNL1
    nsv6562568inversion1nstd223human GRCh38 chr6: 29,766,029-31,471,345 , GRCh37.p13 chr6: 29,733,806-31,439,122 HCG4P9, LINC01149, 126 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
    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
    nsv5469013copy number variation1nstd206human GRCh38 chr6: 30,542,921-30,542,984 , GRCh37.p13 chr6: 30,510,698-30,510,761 GNL1
    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
    nsv5233554copy number variation1nstd204human GRCh38.p13 chr6: 30,467,101-30,998,400 , GRCh37.p13 chr6: 30,434,878-30,966,177 IER3, DHX16, 37 more genes
    nsv5230420copy number variation1nstd204human GRCh38.p13 chr6: 30,504,101-30,658,200 , GRCh37.p13 chr6: 30,471,878-30,625,977 PTMAP1, DHX16, 10 more genes
    nsv5222466copy number variation1nstd204human GRCh38.p13 chr6: 30,539,668-30,541,667 , GRCh37.p13 chr6: 30,507,445-30,509,444 GNL1
    nsv5172493mobile element insertion1nstd203human GRCh38 chr6: 30,550,565-30,550,583 , GRCh37.p13 chr6: 30,518,342-30,518,360 GNL1
    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
    nsv4680231copy number variation1nstd189human GRCh37.p13 chr6: 30,445,766-30,601,174 , GRCh38.p12 chr6: 30,477,989-30,633,397 ABCF1, GNL1, 10 more genes
    nsv4680000copy number variation1nstd189human GRCh37.p13 chr6: 30,496,372-30,638,995 , GRCh38.p12 chr6: 30,528,595-30,671,218 ABCF1, GNL1, 9 more genes
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