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Items: 1 to 20 of 105

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7053830inversion1nstd229human GRCh38 chr6: 29,164,448-38,692,657 , GRCh37.p13 chr6: 29,132,225-38,660,433 GTF2H4, RNF8, 472 more genes
    nsv6782441copy number variation1nstd229human GRCh38 chr6: 29,455,092-29,455,275 , GRCh37.p13 chr6: 29,422,869-29,423,052 OR2H1, LOC105379641, 1 more genes
    nsv6781984copy number variation1nstd229human GRCh38 chr6: 29,460,506-29,464,946 , GRCh37.p13 chr6: 29,428,283-29,432,723 OR2H1, UBDP1
    nsv6779338copy number variation1nstd229human GRCh38 chr6: 29,419,464-29,620,038 , GRCh37.p13 chr6: 29,387,241-29,587,815 GABBR1, RPL13AP, 19 more genes
    nsv6636314copy number variation1nstd102humanUncertain significance GRCh37 chr6: 29,162,783-30,236,331 , GRCh38.p12 chr6: 29,195,006-30,268,554 LOC353009, OR2H2, 92 more genes
    nsv6563406inversion1nstd223human GRCh38 chr6: 25,888,425-29,704,317 , GRCh37.p13 chr6: 25,888,653-29,672,094 OR1F12P, H4C2, 362 more genes
    nsv6397690copy number variation1nstd223human GRCh38 chr6: 29,460,505-29,464,947 , GRCh37.p13 chr6: 29,428,282-29,432,724 UBDP1, OR2H1
    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
    nsv6260683mobile element insertion1nstd215human GRCh38 chr6: 29,460,815-29,460,815 , GRCh37.p13 chr6: 29,428,592-29,428,592 OR2H1
    nsv6135508copy number variation1nstd213human GRCh37 chr6: 27,710,000-30,110,001 , GRCh38.p12 chr6: 27,742,221-30,142,224 GABBR1, H1-5, 224 more genes
    nsv6080386insertion1nstd212human GRCh38 chr6: 29,460,800-29,460,800 , GRCh37.p13 chr6: 29,428,577-29,428,577 OR2H1
    nsv5688225mobile element insertion2nstd211human GRCh38 chr6: 29,460,815-29,460,815 , GRCh37.p13 chr6: 29,428,592-29,428,592 OR2H1
    nsv5402666mobile element insertion1nstd206human GRCh38 chr6: 29,460,815-29,460,866 , GRCh37.p13 chr6: 29,428,592-29,428,643 OR2H1
    nsv5119539mobile element insertion1nstd203human GRCh38 chr6: 29,456,187-29,456,211 , GRCh37.p13 chr6: 29,423,964-29,423,988 OR2H1, OR5V1, 1 more genes
    nsv5105757mobile element insertion1nstd203human GRCh38 chr6: 29,460,800-29,460,815 , GRCh37.p13 chr6: 29,428,577-29,428,592 OR2H1
    nsv5036471inversion1nstd200human GRCh38 chr6: 25,888,426-29,704,316 , GRCh37.p13 chr6: 25,888,654-29,672,093 , OR11A1, 368 more genes
    nsv4879678inversion1nstd200human GRCh37 chr6: 25,888,654-29,672,093 , GRCh38.p12 chr6: 25,888,426-29,704,316 , H1-4, 368 more genes
    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
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