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Items: 1 to 20 of 529

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5953126insertion1nstd209human GRCh38 chr7: 76,017,866-76,017,866 , GRCh37.p13 chr7: 75,647,184-75,647,184 , GRCh37.p13 chr7|NW_003871064.1: 3,547,102-3,547,102 STYXL1
    nsv5924454copy number variation1nstd209human GRCh38 chr7: 76,038,692-76,039,341 , GRCh37.p13 chr7|NW_003871064.1: 3,567,928-3,568,577 , GRCh37.p13 chr7: 75,668,010-75,668,659 STYXL1
    nsv5916825copy number variation1nstd209human GRCh38 chr7: 76,035,312-76,038,488 , GRCh37.p13 chr7|NW_003871064.1: 3,564,548-3,567,724 , GRCh37.p13 chr7: 75,664,630-75,667,806 STYXL1
    nsv5911734copy number variation1nstd209human GRCh38 chr7: 76,034,975-76,038,488 , GRCh37.p13 chr7: 75,664,293-75,667,806 , GRCh37.p13 chr7|NW_003871064.1: 3,564,211-3,567,724 STYXL1
    nsv5857702copy number variation1nstd209human GRCh38 chr7: 76,034,962-76,038,511 , GRCh37.p13 chr7: 75,664,280-75,667,829 , GRCh37.p13 chr7|NW_003871064.1: 3,564,198-3,567,747 STYXL1
    nsv5579930copy number variation1nstd207human GRCh38 chr7: 76,034,977-76,035,208 , GRCh37.p13 chr7|NW_003871064.1: 3,564,213-3,564,444 , GRCh37.p13 chr7: 75,664,295-75,664,526 STYXL1
    nsv5579267copy number variation1nstd207human GRCh38 chr7: 76,038,692-76,039,341 , GRCh37.p13 chr7: 75,668,010-75,668,659 , GRCh37.p13 chr7|NW_003871064.1: 3,567,928-3,568,577 STYXL1
    nsv5574153copy number variation1nstd207human GRCh38 chr7: 76,035,312-76,038,488 , GRCh37.p13 chr7|NW_003871064.1: 3,564,548-3,567,724 , GRCh37.p13 chr7: 75,664,630-75,667,806 STYXL1
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5556455sequence alteration1nstd206human GRCh38 chr7: 76,034,973-76,038,489 , GRCh37.p13 chr7: 75,664,291-75,667,807 , GRCh37.p13 chr7|NW_003871064.1: 3,564,209-3,567,725 STYXL1
    nsv5493289copy number variation1nstd206human GRCh38 chr7: 76,020,665-76,020,956 , GRCh37.p13 chr7|NW_003871064.1: 3,549,901-3,550,192 , GRCh37.p13 chr7: 75,649,983-75,650,274 STYXL1
    nsv5492458copy number variation1nstd206human GRCh38 chr7: 76,031,580-76,045,602 , GRCh37.p13 chr7|NW_003871064.1: 3,560,816-3,574,838 , GRCh37.p13 chr7: 75,660,898-75,674,920 STYXL1
    nsv5490966copy number variation1nstd206human GRCh38 chr7: 76,038,423-76,039,323 , GRCh37.p13 chr7: 75,667,741-75,668,641 , GRCh37.p13 chr7|NW_003871064.1: 3,567,659-3,568,559 STYXL1
    nsv5490787copy number variation1nstd206human GRCh37.p13 chr7|NW_003871064.1: 3,443,117-3,565,522 , GRCh38 chr7: 75,913,881-76,036,286 , GRCh37.p13 chr7: 75,543,199-75,665,604 POR, STYXL1, 4 more genes
    nsv5484765copy number variation1nstd206human GRCh38 chr7: 76,032,378-76,033,833 , GRCh37.p13 chr7: 75,661,696-75,663,151 , GRCh37.p13 chr7|NW_003871064.1: 3,561,614-3,563,069 STYXL1
    nsv5479466copy number variation1nstd206human GRCh38 chr7: 76,045,670-76,062,036 , GRCh37.p13 chr7: 75,674,988-75,691,354 , GRCh37.p13 chr7|NW_003871064.1: 3,574,906-3,591,272 MDH2, STYXL1
    nsv5479103copy number variation1nstd206human GRCh38 chr7: 76,004,483-76,006,915 , GRCh37.p13 chr7|NW_003871064.1: 3,533,719-3,536,151 , GRCh37.p13 chr7: 75,633,801-75,636,233 STYXL1
    nsv5478915copy number variation1nstd206human GRCh38 chr7: 76,039,148-76,039,809 , GRCh37.p13 chr7|NW_003871064.1: 3,568,384-3,569,045 , GRCh37.p13 chr7: 75,668,466-75,669,127 STYXL1
    nsv5476446copy number variation1nstd206human GRCh38 chr7: 75,993,001-75,999,745 , GRCh37.p13 chr7: 75,622,319-75,629,063 , GRCh37.p13 chr7|NW_003871064.1: 3,522,237-3,528,981 TMEM120A, STYXL1
    nsv5475551copy number variation1nstd206human GRCh38 chr7: 76,038,442-76,038,948 , GRCh37.p13 chr7: 75,667,760-75,668,266 , GRCh37.p13 chr7|NW_003871064.1: 3,567,678-3,568,184 STYXL1
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