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Items: 1 to 20 of 180

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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
    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
    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
    nsv6567013inversion1nstd223human GRCh38 chr6: 30,308,865-30,310,465 , GRCh37.p13 chr6: 30,276,642-30,278,242 HCG18, HCG17
    nsv6562568inversion1nstd223human GRCh38 chr6: 29,766,029-31,471,345 , GRCh37.p13 chr6: 29,733,806-31,439,122 HCG4P9, LINC01149, 126 more genes
    nsv6559040inversion1nstd223human GRCh38 chr6: 30,295,396-30,298,074 , GRCh37.p13 chr6: 30,263,173-30,265,851 HCG18, HCG17
    nsv6413811copy number variation1nstd223human GRCh38 chr6: 30,326,301-30,328,100 , GRCh37.p13 chr6: 30,294,078-30,295,877 HCG17, TRIM39, 2 more genes
    nsv6411255copy number variation1nstd223human GRCh38 chr6: 30,281,678-30,287,536 , GRCh37.p13 chr6: 30,249,455-30,255,313 HCG18, HCG17
    nsv6410379copy number variation1nstd223human GRCh38 chr6: 30,299,426-30,302,141 , GRCh37.p13 chr6: 30,267,203-30,269,918 HCG18, HCG17
    nsv6397160copy number variation1nstd223human GRCh38 chr6: 30,289,908-30,322,966 , GRCh37.p13 chr6: 30,257,685-30,290,743 HCG17, HCG18
    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
    nsv6260699mobile element insertion1nstd215human GRCh38 chr6: 30,320,789-30,320,789 , GRCh37.p13 chr6: 30,288,566-30,288,566 HCG18, HCG17
    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
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