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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098844copy number variation1nstd102humanUncertain significance GRCh37 chr2: 65,296,579-71,305,638 , GRCh38.p12 chr2: 65,069,445-71,078,508 SNRNP27, TEX261, 121 more genes
    nsv6677446copy number variation1nstd229human GRCh38 chr2: 65,735,801-65,759,200 , GRCh37.p13 chr2: 65,962,935-65,986,334 LOC105369167
    nsv6675787copy number variation1nstd229human GRCh38 chr2: 65,710,172-65,731,891 , GRCh37.p13 chr2: 65,937,306-65,959,025 LOC105369167
    nsv6673965copy number variation1nstd229human GRCh38 chr2: 65,696,260-65,730,413 , GRCh37.p13 chr2: 65,923,394-65,957,547 LOC105369167
    nsv6668317copy number variation1nstd229human GRCh38 chr2: 65,734,001-65,766,000 , GRCh37.p13 chr2: 65,961,135-65,993,134 LOC105369167
    nsv6664504copy number variation1nstd229human GRCh38 chr2: 65,555,879-65,811,285 , GRCh37.p13 chr2: 65,783,013-66,038,419 VTRNA2-2P, LOC105369167, 2 more genes
    nsv6663754copy number variation1nstd229human GRCh38 chr2: 65,685,001-65,809,300 , GRCh37.p13 chr2: 65,912,135-66,036,434 LOC105369167
    nsv6661913copy number variation1nstd229human GRCh38 chr2: 65,710,818-66,368,117 , GRCh37.p13 chr2: 65,937,952-66,595,249 LINC02934, MIR4778, 3 more genes
    nsv6659301copy number variation1nstd229human GRCh38 chr2: 65,744,047-65,748,671 , GRCh37.p13 chr2: 65,971,181-65,975,805 LOC105369167
    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
    nsv6551094inversion1nstd223human GRCh38 chr2: 64,078,330-67,334,177 , GRCh37.p13 chr2: 64,305,464-67,561,309 LINC01805, LINC02579, 59 more genes
    nsv6350621copy number variation1nstd223human GRCh38 chr2: 65,555,879-65,811,282 , GRCh37.p13 chr2: 65,783,013-66,038,416 LOC107985889, VTRNA2-2P, 2 more genes
    nsv6346768copy number variation1nstd223human GRCh38 chr2: 65,744,047-65,748,666 , GRCh37.p13 chr2: 65,971,181-65,975,800 LOC105369167
    nsv6344524copy number variation1nstd223human GRCh38 chr2: 65,741,451-65,741,686 , GRCh37.p13 chr2: 65,968,585-65,968,820 LOC105369167
    nsv6342146copy number variation1nstd223human GRCh38 chr2: 65,696,260-65,730,406 , GRCh37.p13 chr2: 65,923,394-65,957,540 LOC105369167
    nsv6336806copy number variation1nstd223human GRCh38 chr2: 65,734,440-65,762,264 , GRCh37.p13 chr2: 65,961,574-65,989,398 LOC105369167
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6314726copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 40,607,042-146,902,764 , GRCh38.p12 chr2: 40,379,902-146,145,196 ACTG2, ACYP2, 1713 more genes
    nsv6292495mobile element insertion1nstd186human GRCh37 chr2: 65,967,071-65,967,122 , GRCh38.p12 chr2: 65,739,937-65,739,988 LOC105369167
    nsv6252537mobile element insertion1nstd215human GRCh38 chr2: 65,745,927-65,745,927 , GRCh37.p13 chr2: 65,973,061-65,973,061 LOC105369167
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