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Items: 1 to 20 of 132

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7057262inversion1nstd229human GRCh38 chr6: 30,724,123-30,725,176 , GRCh37.p13 chr6: 30,691,900-30,692,953 TUBB
    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
    nsv7045112inversion1nstd229human GRCh38 chr6: 30,561,326-37,907,708 , GRCh37.p13 chr6: 30,529,103-37,875,484 ZBTB22, PNPLA1, 355 more genes
    nsv6795700copy number variation1nstd229human GRCh38 chr6: 30,611,001-30,837,400 , GRCh37.p13 chr6: 30,578,778-30,805,177 PPP1R18, C6orf136, 16 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
    nsv6795605copy number variation1nstd229human GRCh38 chr6: 30,725,118-30,725,638 , GRCh37.p13 chr6: 30,692,895-30,693,415 TUBB
    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
    nsv6630969copy number variation1nstd224human GRCh37 chr6: 30,688,427-30,753,146 , GRCh38.p12 chr6: 30,720,650-30,785,369 IER3, FLOT1, 4 more genes
    nsv6562568inversion1nstd223human GRCh38 chr6: 29,766,029-31,471,345 , GRCh37.p13 chr6: 29,733,806-31,439,122 HCG4P9, LINC01149, 126 more genes
    nsv6402081copy number variation1nstd223human GRCh38 chr6: 30,724,101-30,725,400 , GRCh37.p13 chr6: 30,691,878-30,693,177 TUBB
    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
    nsv5378350translocation1nstd200human GRCh38 chr8: 133,982,808-133,982,808 , GRCh38 chr6: 30,725,179-30,725,179 , GRCh37.p13 chr6: 30,692,956-30,692,956 , GRCh37.p13 chr8: 134,995,051-134,995,051 TUBB
    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
    nsv5227962copy number variation1nstd204human GRCh38.p13 chr6: 30,724,114-30,725,413 , GRCh37.p13 chr6: 30,691,891-30,693,190 TUBB
    nsv5222123copy number variation1nstd204human GRCh38.p13 chr6: 30,723,069-30,725,413 , GRCh37.p13 chr6: 30,690,846-30,693,190 TUBB
    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
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