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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
    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
    nsv6788480copy number variation1nstd229human GRCh38 chr6: 30,212,901-30,229,100 , GRCh37.p13 chr6: 30,180,678-30,196,877 TRIM26
    nsv6787769copy number variation1nstd229human GRCh38 chr6: 30,206,507-30,211,281 , GRCh37.p13 chr6: 30,174,284-30,179,058 TRIM26
    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
    nsv6562568inversion1nstd223human GRCh38 chr6: 29,766,029-31,471,345 , GRCh37.p13 chr6: 29,733,806-31,439,122 HCG4P9, LINC01149, 126 more genes
    nsv6302202copy number variation1nstd186human GRCh37 chr6: 30,155,423-30,155,723 , GRCh38.p12 chr6: 30,187,646-30,187,946 PAIP1P1, TRIM26
    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
    nsv6267720copy number variation1nstd214human GRCh38 chr6: 30,193,062-30,193,119 , GRCh37.p13 chr6: 30,160,839-30,160,896 TRIM26
    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
    nsv6070742insertion1nstd212human GRCh38 chr6: 30,183,383-30,183,383 , GRCh37.p13 chr6: 30,151,160-30,151,160 TRIM26
    nsv5958497insertion1nstd209human GRCh38 chr6: 30,183,383-30,183,383 , GRCh37.p13 chr6: 30,151,160-30,151,160 TRIM26
    nsv5635440insertion1nstd207human GRCh38 chr6: 30,183,383-30,183,383 , GRCh37.p13 chr6: 30,151,160-30,151,160 TRIM26
    nsv5578658copy number variation1nstd207human GRCh38 chr6: 30,187,913-30,188,212 , GRCh37.p13 chr6: 30,155,690-30,155,989 TRIM26, PAIP1P1
    nsv5576041copy number variation1nstd207human GRCh38 chr6: 30,208,318-30,208,660 , GRCh37.p13 chr6: 30,176,095-30,176,437 TRIM26
    nsv5544046insertion1nstd206human GRCh38 chr6: 30,183,383-30,183,383 , GRCh37.p13 chr6: 30,151,160-30,151,160 TRIM26
    nsv5466448copy number variation1nstd206human GRCh38 chr6: 30,187,626-30,187,966 , GRCh37.p13 chr6: 30,155,403-30,155,743 PAIP1P1, TRIM26
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