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Items: 1 to 20 of 173

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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
    nsv7040769inversion1nstd229human GRCh38 chr6: 31,172,178-31,172,280 , GRCh37.p13 chr6: 31,139,955-31,140,057 PSORS1C3
    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
    nsv6783952copy number variation1nstd229human GRCh38 chr6: 31,140,741-31,322,974 , GRCh37.p13 chr6: 31,108,518-31,290,751 PSORS1C3, POLR2LP1, 10 more genes
    nsv6779841copy number variation1nstd229human GRCh38 chr6: 31,173,219-31,176,176 , GRCh37.p13 chr6: 31,140,996-31,143,953 PSORS1C3
    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
    nsv6260703mobile element insertion1nstd215human GRCh38 chr6: 31,183,543-31,183,543 , GRCh37.p13 chr6: 31,151,320-31,151,320 PSORS1C3
    nsv6135918copy number variation1nstd213human GRCh37 chr6: 30,870,000-31,240,001 , GRCh38.p12 chr6: 30,902,223-31,272,224 CDSN, GTF2H4, 19 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
    nsv6065029insertion1nstd212human GRCh38 chr6: 31,183,535-31,183,535 , GRCh37.p13 chr6: 31,151,312-31,151,312 PSORS1C3
    nsv5901873copy number variation1nstd209human GRCh38 chr6: 31,180,975-31,181,294 , GRCh37.p13 chr6: 31,148,752-31,149,071 PSORS1C3
    nsv5460471copy number variation1nstd206human GRCh38 chr6: 31,119,831-31,186,318 , GRCh37.p13 chr6: 31,087,608-31,154,095 CDSN, POU5F1, 6 more genes
    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
    nsv4828596copy number variation1nstd200human GRCh37 chr6: 31,087,555-31,154,139 , GRCh38.p12 chr6: 31,119,778-31,186,362 PSORS1C3, POU5F1, 6 more genes
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