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Items: 1 to 20 of 212

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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
    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
    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
    nsv6785277copy number variation1nstd229human GRCh38 chr6: 30,826,057-30,835,862 , GRCh37.p13 chr6: 30,793,834-30,803,639 LINC00243
    nsv6779587copy number variation1nstd229human GRCh38 chr6: 30,807,315-30,815,894 , GRCh37.p13 chr6: 30,775,092-30,783,671 LINC00243
    nsv6631155copy number variation1nstd224human GRCh37 chr6: 30,735,105-30,789,647 , GRCh38.p12 chr6: 30,767,328-30,821,870 LINC00243, HCG20
    nsv6562568inversion1nstd223human GRCh38 chr6: 29,766,029-31,471,345 , GRCh37.p13 chr6: 29,733,806-31,439,122 HCG4P9, LINC01149, 126 more genes
    nsv6408695copy number variation1nstd223human GRCh38 chr6: 30,801,388-30,816,861 , GRCh37.p13 chr6: 30,769,165-30,784,638 LINC00243
    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
    nsv6268575copy number variation1nstd214human GRCh38 chr6: 30,815,755-30,815,912 , GRCh37.p13 chr6: 30,783,532-30,783,689 LINC00243
    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
    nsv6063435insertion1nstd212human GRCh38 chr6: 30,815,375-30,815,375 , GRCh37.p13 chr6: 30,783,152-30,783,152 LINC00243
    nsv6018575copy number variation1nstd212human GRCh38 chr6: 30,815,765-30,815,924 , GRCh37.p13 chr6: 30,783,542-30,783,701 LINC00243
    nsv5627011insertion1nstd207human GRCh38 chr6: 30,815,371-30,815,371 , GRCh37.p13 chr6: 30,783,148-30,783,148 LINC00243
    nsv5577804copy number variation1nstd207human GRCh38 chr6: 30,815,711-30,815,870 , GRCh37.p13 chr6: 30,783,488-30,783,647 LINC00243
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