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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6290857copy number variation1nstd102humanUncertain significance GRCh37 chr2: 230,581,849-230,696,659 , GRCh38.p12 chr2: 229,717,133-229,831,943 TRIP12
    nsv6290944copy number variation1nstd102humanUncertain significance GRCh37 chr2: 230,626,876-230,734,232 , GRCh38.p12 chr2: 229,762,160-229,869,516 TRIP12
    nsv4450540copy number variation1nstd102humanUncertain significance GRCh37 chr2: 230,622,100-230,720,254 , GRCh38.p12 chr2: 229,757,384-229,855,538 TRIP12
    nsv4450356copy number variation1nstd102humanUncertain significance GRCh37 chr2: 230,588,429-230,667,704 , GRCh38.p12 chr2: 229,723,713-229,802,988 TRIP12
    nsv4449737copy number variation1nstd102humanPathogenic GRCh37 chr2: 230,769,636-230,792,670 , GRCh38.p12 chr2: 229,904,920-229,927,954 TRIP12, FBXO36
    nsv4454720copy number variation1nstd102humanUncertain significance GRCh37 chr2: 230,487,853-230,709,082 , GRCh38.p12 chr2: 229,623,137-229,844,366 TRIP12, DNER
    nsv4452955copy number variation1nstd102humanUncertain significance GRCh37 chr2: 230,491,545-230,657,293 , GRCh38.p12 chr2: 229,626,829-229,792,577 TRIP12, DNER
    nsv4451620copy number variation1nstd102humanUncertain significance GRCh37 chr2: 230,612,450-230,770,381 , GRCh38.p12 chr2: 229,747,734-229,905,665 TRIP12, RNU6-613P
    nsv4452591copy number variation1nstd102humanUncertain significance GRCh37 chr2: 230,566,834-230,689,317 , GRCh38.p12 chr2: 229,702,118-229,824,601 TRIP12, DNER
    nsv6291260copy number variation1nstd102humanPathogenic GRCh37 chr2: 230,689,315-230,810,845 , GRCh38.p12 chr2: 229,824,599-229,946,129 TRIP12, RNU6-613P, 2 more genes
    nsv3318984copy number variation1nstd45humanPathogenic GRCh38.p12 chr2: 229,763,837-229,922,009 , GRCh37 chr2: 230,628,553-230,786,725 TRIP12, FBXO36, 1 more genes
    nsv3889477copy number variation1nstd102humanBenign GRCh37 chr2: 230,763,690-230,879,345 , GRCh38.p12 chr2: 229,898,974-230,014,629 TRIP12, LOC105373924, 3 more genes
    nsv3905887copy number variation1nstd102humanLikely benign GRCh37 chr2: 230,643,557-230,833,931 , GRCh38 chr2: 229,778,841-229,969,215 , NCBI36 chr2: 230,351,801-230,542,175 TRIP12, LOC105373924, 3 more genes
    nsv6637011copy number variation1nstd102humanUncertain significance GRCh37 chr2: 230,751,471-230,789,873 , GRCh38.p12 chr2: 229,886,755-229,925,157 TRIP12, RNU6-613P, 1 more genes
    nsv4674791copy number variation1nstd102humanUncertain significance GRCh37 chr2: 230,491,430-230,775,587 , GRCh38.p12 chr2: 229,626,714-229,910,871 TRIP12, DNER, 1 more genes
    nsv3910314copy number variation1nstd102humanUncertain significance NCBI36 chr2: 230,290,711-230,509,263 , GRCh37.p13 chr2: 230,582,467-230,801,019 , GRCh38.p12 chr2: 229,717,751-229,936,303 TRIP12, RNU6-613P, 2 more genes
    nsv4453540copy number variation1nstd102humanUncertain significance GRCh37 chr2: 230,573,487-230,764,226 , GRCh38.p12 chr2: 229,708,771-229,899,510 TRIP12, RNU6-613P, 1 more genes
    nsv4450804copy number variation1nstd102humanUncertain significance GRCh37 chr2: 230,653,628-230,835,177 , GRCh38.p12 chr2: 229,788,912-229,970,461 TRIP12, FBXO36, 3 more genes
    nsv4674537copy number variation1nstd102humanPathogenic GRCh37 chr2: 230,626,876-230,887,430 , GRCh38.p12 chr2: 229,762,160-230,022,714 TRIP12, FBXO36, 4 more genes
    nsv4452033copy number variation1nstd102humanPathogenic GRCh37 chr2: 230,622,100-230,870,340 , GRCh38.p12 chr2: 229,757,384-230,005,624 TRIP12, FBXO36, 4 more genes
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