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Items: 1 to 20 of 348

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7057750inversion1nstd229human GRCh38 chr3: 16,097,213-16,312,328 , GRCh37.p13 chr3: 16,138,720-16,353,835 GALNT15, DPH3, 3 more genes
    nsv7055896inversion1nstd229human GRCh38 chr3: 16,300,028-16,305,156 , GRCh37.p13 chr3: 16,341,535-16,346,663 LOC107986065, OXNAD1
    nsv7049810inversion1nstd229human GRCh38 chr3: 16,139,271-16,577,361 , GRCh37.p13 chr3: 16,180,778-16,618,868 OXNAD1, LINC00690, 5 more genes
    nsv7040393inversion1nstd229human GRCh38 chr3: 16,301,450-16,312,161 , GRCh37.p13 chr3: 16,342,957-16,353,668 LOC107986065, OXNAD1
    nsv6716888copy number variation1nstd229human GRCh38 chr3: 16,076,014-16,572,211 , GRCh37.p13 chr3: 16,117,521-16,613,718 OXNAD1, LOC107986065, 5 more genes
    nsv6714113copy number variation1nstd229human GRCh38 chr3: 16,318,257-16,321,294 , GRCh37.p13 chr3: 16,359,764-16,362,801 RFTN1, OXNAD1
    nsv6713729copy number variation1nstd229human GRCh38 chr3: 16,329,679-16,336,725 , GRCh37.p13 chr3: 16,371,186-16,378,232 RFTN1, OXNAD1
    nsv6713146copy number variation1nstd229human GRCh38 chr3: 16,338,031-16,338,096 , GRCh37.p13 chr3: 16,379,538-16,379,603 OXNAD1, RFTN1
    nsv6713100copy number variation1nstd229human GRCh38 chr3: 15,359,925-17,364,956 , GRCh37.p13 chr3: 15,401,432-17,406,448 RNU6-1024P, COLQ, 27 more genes
    nsv6713016copy number variation1nstd229human GRCh38 chr3: 16,314,722-16,317,205 , GRCh37.p13 chr3: 16,356,229-16,358,712 OXNAD1, RFTN1
    nsv6712172copy number variation1nstd229human GRCh38 chr3: 16,315,472-16,315,509 , GRCh37.p13 chr3: 16,356,979-16,357,016 RFTN1, OXNAD1
    nsv6709847copy number variation1nstd229human GRCh38 chr3: 16,297,154-16,301,389 , GRCh37.p13 chr3: 16,338,661-16,342,896 LOC107986065, OXNAD1
    nsv6708818copy number variation1nstd229human GRCh38 chr3: 16,280,773-16,283,241 , GRCh37.p13 chr3: 16,322,280-16,324,748 OXNAD1
    nsv6707828copy number variation1nstd229human GRCh38 chr3: 16,366,195-16,366,233 , GRCh37.p13 chr3: 16,407,702-16,407,740 OXNAD1, RFTN1
    nsv6707740copy number variation1nstd229human GRCh38 chr3: 16,332,401-16,339,100 , GRCh37.p13 chr3: 16,373,908-16,380,607 OXNAD1, RFTN1
    nsv6707436copy number variation1nstd229human GRCh38 chr3: 16,318,439-16,323,233 , GRCh37.p13 chr3: 16,359,946-16,364,740 OXNAD1, RFTN1
    nsv6706523copy number variation1nstd229human GRCh38 chr3: 16,357,982-16,366,261 , GRCh37.p13 chr3: 16,399,489-16,407,768 RFTN1, OXNAD1
    nsv6706489copy number variation1nstd229human GRCh38 chr3: 16,348,978-16,349,068 , GRCh37.p13 chr3: 16,390,485-16,390,575 OXNAD1, RFTN1
    nsv6704672copy number variation1nstd229human GRCh38 chr3: 15,918,468-16,474,227 , GRCh37.p13 chr3: 15,959,975-16,515,734 RFTN1, DPH3, 5 more genes
    nsv6704254copy number variation1nstd229human GRCh38 chr3: 16,387,380-16,407,005 , GRCh37.p13 chr3: 16,428,887-16,448,512 RFTN1, OXNAD1
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