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Items: 1 to 20 of 362

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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
    nsv7046539inversion1nstd229human GRCh38 chr6: 30,085,556-30,247,878 , GRCh37.p13 chr6: 30,053,333-30,215,655 TRIM15, TRIM26BP, 7 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
    nsv7041334inversion1nstd229human GRCh38 chr6: 29,474,330-30,422,378 , GRCh37.p13 chr6: 29,442,107-30,390,155 HCG4, HLA-F, 80 more genes
    nsv6795437copy number variation1nstd229human GRCh38 chr6: 30,307,918-30,308,524 , GRCh37.p13 chr6: 30,275,695-30,276,301 HCG18, HCG17
    nsv6794079copy number variation1nstd229human GRCh38 chr6: 30,287,582-30,290,374 , GRCh37.p13 chr6: 30,255,359-30,258,151 HCG18, HCG17
    nsv6793933copy number variation1nstd229human GRCh38 chr6: 30,316,721-30,316,865 , GRCh37.p13 chr6: 30,284,498-30,284,642 HCG17, HCG18
    nsv6790569copy number variation1nstd229human GRCh38 chr6: 30,325,461-30,326,008 , GRCh37.p13 chr6: 30,293,238-30,293,785 TRIM39, HCG17, 1 more genes
    nsv6789205copy number variation1nstd229human GRCh38 chr6: 30,281,678-30,287,539 , GRCh37.p13 chr6: 30,249,455-30,255,316 HCG17, HCG18
    nsv6789204copy number variation1nstd229human GRCh38 chr6: 30,244,634-30,248,419 , GRCh37.p13 chr6: 30,212,411-30,216,196 HCG17
    nsv6785903copy number variation1nstd229human GRCh38 chr6: 30,238,828-30,241,692 , GRCh37.p13 chr6: 30,206,605-30,209,469 TRIM26BP, HCG17
    nsv6785768copy number variation1nstd229human GRCh38 chr6: 30,304,511-30,308,304 , GRCh37.p13 chr6: 30,272,288-30,276,081 HCG17, HCG18
    nsv6785588copy number variation1nstd229human GRCh38 chr6: 30,296,403-30,301,788 , GRCh37.p13 chr6: 30,264,180-30,269,565 HCG17, HCG18
    nsv6784630copy number variation1nstd229human GRCh38 chr6: 30,262,744-30,262,817 , GRCh37.p13 chr6: 30,230,521-30,230,594 HCG17, HLA-L
    nsv6636358copy number variation1nstd102humanUncertain significance GRCh37 chr6: 29,730,504-30,202,199 , GRCh38.p12 chr6: 29,762,727-30,234,422 HCG4P8, HLA-V, 45 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
    nsv6631033copy number variation1nstd224human GRCh37 chr6: 30,202,571-30,215,592 , GRCh38.p12 chr6: 30,234,794-30,247,815 TRIM26BP, HCG17
    nsv6567013inversion1nstd223human GRCh38 chr6: 30,308,865-30,310,465 , GRCh37.p13 chr6: 30,276,642-30,278,242 HCG18, HCG17
    nsv6565515inversion1nstd223human GRCh38 chr6: 30,237,290-30,237,952 , GRCh37.p13 chr6: 30,205,067-30,205,729 TRIM26BP, HCG17
    nsv6562568inversion1nstd223human GRCh38 chr6: 29,766,029-31,471,345 , GRCh37.p13 chr6: 29,733,806-31,439,122 HCG4P9, LINC01149, 126 more genes
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