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Items: 1 to 20 of 193

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5880757copy number variation1nstd209human GRCh38 chr1: 156,328,014-156,328,094 , GRCh37.p13 chr1: 156,297,805-156,297,885 CCT3
    nsv5867942copy number variation1nstd209human GRCh38 chr1: 156,329,846-156,330,570 , GRCh37.p13 chr1: 156,299,637-156,300,361 CCT3
    nsv5686864mobile element insertion1nstd211human GRCh38 chr1: 156,334,647-156,334,647 , GRCh37.p13 chr1: 156,304,438-156,304,438 CCT3
    nsv5619012insertion1nstd207human GRCh38 chr1: 156,328,045-156,328,045 , GRCh37.p13 chr1: 156,297,836-156,297,836 CCT3
    nsv5584387copy number variation1nstd207human GRCh38 chr1: 156,329,730-156,330,454 , GRCh37.p13 chr1: 156,299,521-156,300,245 CCT3
    nsv5559729sequence alteration1nstd206human GRCh38 chr1: 156,338,639-156,344,748 , GRCh37.p13 chr1: 156,308,430-156,314,539 CCT3, TSACC
    nsv5548391insertion1nstd206human GRCh38 chr1: 156,328,045-156,328,045 , GRCh37.p13 chr1: 156,297,836-156,297,836 CCT3
    nsv5429445copy number variation1nstd206human GRCh38 chr1: 156,331,975-156,332,093 , GRCh37.p13 chr1: 156,301,766-156,301,884 CCT3
    nsv5421966copy number variation1nstd206human GRCh38 chr1: 156,327,875-156,327,943 , GRCh37.p13 chr1: 156,297,666-156,297,734 CCT3
    nsv5421884copy number variation1nstd206human GRCh38 chr1: 156,321,025-156,354,439 , GRCh37.p13 chr1: 156,290,816-156,324,230 TSACC, CCT3
    nsv5419573copy number variation1nstd206human GRCh38 chr1: 156,329,765-156,330,455 , GRCh37.p13 chr1: 156,299,556-156,300,246 CCT3
    nsv5401455mobile element insertion1nstd206human GRCh38 chr1: 156,334,647-156,334,682 , GRCh37.p13 chr1: 156,304,438-156,304,473 CCT3
    nsv5381285copy number variation2nstd102humanUncertain significance GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699 , DCST1, 2428 more genes
    nsv5342001translocation1nstd200human GRCh37 chr1: 156,301,766-156,301,766 , GRCh37 chr1: 156,301,884-156,301,884 , GRCh38.p12 chr1: 156,331,975-156,331,975 , GRCh38.p12 chr1: 156,332,093-156,332,093 CCT3
    nsv5296489copy number variation1nstd204human GRCh37.p13 chr1: 156,306,480-156,306,591 , GRCh38.p13 chr1: 156,336,689-156,336,800 CCT3, TSACC
    nsv5282521copy number variation1nstd204human GRCh38.p13 chr1: 156,331,965-156,332,102 , GRCh37.p13 chr1: 156,301,756-156,301,893 CCT3
    nsv5209284copy number variation1nstd204human GRCh38.p13 chr1: 156,136,401-156,327,400 , GRCh37.p13 chr1: 156,106,192-156,297,191 PAQR6, SEMA4A, 10 more genes
    nsv4903927copy number variation1nstd200human GRCh38 chr1: 156,291,691-156,308,597 , GRCh37.p13 chr1: 156,261,482-156,278,388 SMG5, VHLL, 3 more genes
    nsv4897586copy number variation1nstd200human GRCh38 chr1: 156,331,975-156,332,093 , GRCh37.p13 chr1: 156,301,766-156,301,884 CCT3
    nsv4784337copy number variation1nstd200human GRCh37 chr1: 156,299,617-156,300,337 , GRCh38.p12 chr1: 156,329,826-156,330,546 CCT3
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