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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
    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
    nsv6562568inversion1nstd223human GRCh38 chr6: 29,766,029-31,471,345 , GRCh37.p13 chr6: 29,733,806-31,439,122 HCG4P9, LINC01149, 126 more genes
    nsv6412888copy number variation1nstd223human GRCh38 chr6: 31,261,196-31,347,280 , GRCh37.p13 chr6: 31,228,973-31,315,057 WASF5P, LINC02571, 4 more genes
    nsv6412779copy number variation1nstd223human GRCh38 chr6: 31,295,601-31,324,400 , GRCh37.p13 chr6: 31,263,378-31,292,177 LOC112267902, LINC02571
    nsv6410965copy number variation1nstd223human GRCh38 chr6: 31,251,595-31,343,873 , GRCh37.p13 chr6: 31,219,372-31,311,650 HLA-C, RPL3P2, 4 more genes
    nsv6410546copy number variation1nstd223human GRCh38 chr6: 31,251,280-31,343,720 , GRCh37.p13 chr6: 31,219,057-31,311,497 HLA-C, RPL3P2, 4 more genes
    nsv6409444copy number variation1nstd223human GRCh38 chr6: 31,302,101-31,324,200 , GRCh37.p13 chr6: 31,269,878-31,291,977 LINC02571, LOC112267902
    nsv6402860copy number variation1nstd223human GRCh38 chr6: 31,261,410-31,347,322 , GRCh37.p13 chr6: 31,229,187-31,315,099 HLA-C, RPL3P2, 4 more genes
    nsv6400023copy number variation1nstd223human GRCh38 chr6: 31,252,807-31,345,201 , GRCh37.p13 chr6: 31,220,584-31,312,978 USP8P1, LINC02571, 4 more genes
    nsv6399712copy number variation1nstd223human GRCh38 chr6: 31,253,244-31,345,648 , GRCh37.p13 chr6: 31,221,021-31,313,425 HLA-C, RPL3P2, 4 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
    nsv5903601copy number variation1nstd209human GRCh38 chr6: 31,281,922-31,361,743 , GRCh37.p13 chr6: 31,249,699-31,329,520 HLA-B, RPL3P2, 5 more genes
    nsv5900955copy number variation1nstd209human GRCh38 chr6: 31,268,646-31,353,767 , GRCh37.p13 chr6: 31,236,423-31,321,544 HLA-B, HLA-C, 6 more genes
    nsv5900873copy number variation1nstd209human GRCh38 chr6: 31,261,615-31,347,363 , GRCh37.p13 chr6: 31,229,392-31,315,140 HLA-C, RPL3P2, 4 more genes
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