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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096907copy number variation2nstd102humanPathogenic GRCh37 chr2: 72,359,356-74,779,761 , GRCh38.p12 chr2: 72,132,227-74,552,634 RNU6-111P, LOC105374800, 71 more genes
    nsv7096902copy number variation3nstd102humanPathogenic GRCh37 chr2: 71,004,499-74,779,761 , GRCh38.p12 chr2: 70,777,367-74,552,634 TAF13P2, LOC107985897, 100 more genes
    nsv7096520copy number variation1nstd102humanUncertain significance GRCh37 chr2: 69,240,632-74,779,761 , GRCh38.p12 chr2: 69,013,500-74,552,634 LOC112268419, DQX1, 140 more genes
    nsv7050863inversion1nstd229human GRCh38 chr2: 73,088,744-73,091,882 , GRCh37.p13 chr2: 73,315,872-73,319,010 RAB11FIP5
    nsv7045322inversion1nstd229human GRCh38 chr2: 72,990,406-73,359,168 , GRCh37.p13 chr2: 73,217,535-73,586,296 RAB11FIP5, LOC105374802, 12 more genes
    nsv7043822inversion1nstd229human GRCh38 chr2: 73,029,636-73,188,065 , GRCh37.p13 chr2: 73,256,765-73,415,193 RAB11FIP5, SFXN5, 1 more genes
    nsv6678052copy number variation1nstd229human GRCh38 chr2: 72,752,501-73,363,500 , GRCh37.p13 chr2: 72,979,630-73,590,628 NOTO, LOC105374804, 16 more genes
    nsv6676257copy number variation1nstd229human GRCh38 chr2: 73,071,354-73,071,660 , GRCh37.p13 chr2: 73,298,483-73,298,789 SFXN5, RAB11FIP5
    nsv6675246copy number variation1nstd229human GRCh38 chr2: 73,056,556-73,128,239 , GRCh37.p13 chr2: 73,283,685-73,355,367 RAB11FIP5, SFXN5
    nsv6674589copy number variation1nstd229human GRCh38 chr2: 73,098,240-73,109,158 , GRCh37.p13 chr2: 73,325,368-73,336,286 RAB11FIP5
    nsv6672083copy number variation1nstd229human GRCh38 chr2: 73,029,601-73,219,300 , GRCh37.p13 chr2: 73,256,730-73,446,428 NOTO, RAB11FIP5, 3 more genes
    nsv6671362copy number variation1nstd229human GRCh38 chr2: 73,089,701-73,094,100 , GRCh37.p13 chr2: 73,316,829-73,321,228 RAB11FIP5
    nsv6668743copy number variation1nstd229human GRCh38 chr2: 73,089,459-73,105,017 , GRCh37.p13 chr2: 73,316,587-73,332,145 RAB11FIP5
    nsv6664443copy number variation1nstd229human GRCh38 chr2: 72,890,401-73,109,300 , GRCh37.p13 chr2: 73,117,530-73,336,428 EMX1, SPR, 5 more genes
    nsv6664130copy number variation1nstd229human GRCh38 chr2: 73,096,234-73,096,727 , GRCh37.p13 chr2: 73,323,362-73,323,855 RAB11FIP5
    nsv6661112copy number variation1nstd229human GRCh38 chr2: 73,078,121-73,081,615 , GRCh37.p13 chr2: 73,305,249-73,308,743 RAB11FIP5
    nsv6660539copy number variation1nstd229human GRCh38 chr2: 73,093,105-73,104,950 , GRCh37.p13 chr2: 73,320,233-73,332,078 RAB11FIP5
    nsv6659418copy number variation1nstd229human GRCh38 chr2: 73,104,862-73,110,650 , GRCh37.p13 chr2: 73,331,990-73,337,778 RAB11FIP5
    nsv6658891copy number variation1nstd229human GRCh38 chr2: 73,071,920-73,074,907 , GRCh37.p13 chr2: 73,299,049-73,302,035 SFXN5, RAB11FIP5
    nsv6634330copy number variation1nstd102humanPathogenic GRCh37 chr2: 11,504,318-111,365,996 , GRCh38.p12 chr2: 11,364,192-110,608,419 CYP1B1-AS1, LOC107985771, 1649 more genes
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