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Items: 1 to 20 of 359

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148056copy number variation1nstd102humanPathogenic GRCh37 chr2: 186,698,504-223,918,111 , GRCh38.p12 chr2: 185,833,777-223,053,393 DNAJB1P1, MTCO2P17, 580 more genes
    nsv7047325inversion1nstd229human GRCh38 chr2: 197,652,183-197,654,364 , GRCh37.p13 chr2: 198,516,907-198,519,088 RFTN2
    nsv7045795inversion1nstd229human GRCh38 chr2: 195,566,013-199,490,438 , GRCh37.p13 chr2: 196,430,737-200,355,161 LINC01827, LOC107985972, 48 more genes
    nsv7040925inversion1nstd229human GRCh38 chr2: 197,488,353-197,683,233 , GRCh37.p13 chr2: 198,353,077-198,547,957 MOB4, RFTN2, 4 more genes
    nsv6697930copy number variation1nstd229human GRCh38 chr2: 197,421,801-197,612,200 , GRCh37.p13 chr2: 198,286,525-198,476,924 MOB4, HSPE1, 8 more genes
    nsv6697182copy number variation1nstd229human GRCh38 chr2: 192,562,889-202,434,958 , GRCh37.p13 chr2: 193,427,615-203,299,681 RNU6-915P, SLC44A3P1, 150 more genes
    nsv6696721copy number variation1nstd229human GRCh38 chr2: 197,596,194-197,598,877 , GRCh37.p13 chr2: 198,460,918-198,463,601 RFTN2
    nsv6694958copy number variation1nstd229human GRCh38 chr2: 197,650,601-197,657,600 , GRCh37.p13 chr2: 198,515,325-198,522,324 RFTN2
    nsv6694369copy number variation1nstd229human GRCh38 chr2: 197,594,061-197,601,339 , GRCh37.p13 chr2: 198,458,785-198,466,063 RFTN2
    nsv6694315copy number variation1nstd229human GRCh38 chr2: 197,586,844-197,586,979 , GRCh37.p13 chr2: 198,451,568-198,451,703 RFTN2
    nsv6692019copy number variation1nstd229human GRCh38 chr2: 197,653,151-197,657,312 , GRCh37.p13 chr2: 198,517,875-198,522,036 RFTN2
    nsv6691203copy number variation1nstd229human GRCh38 chr2: 197,673,418-197,673,479 , GRCh37.p13 chr2: 198,538,142-198,538,203 RFTN2
    nsv6688889copy number variation1nstd229human GRCh38 chr2: 197,577,598-197,578,071 , GRCh37.p13 chr2: 198,442,322-198,442,795 RFTN2
    nsv6688177copy number variation1nstd229human GRCh38 chr2: 197,589,501-197,592,200 , GRCh37.p13 chr2: 198,454,225-198,456,924 RFTN2
    nsv6687913copy number variation1nstd229human GRCh38 chr2: 197,656,911-197,661,138 , GRCh37.p13 chr2: 198,521,635-198,525,862 RFTN2
    nsv6683036copy number variation1nstd229human GRCh38 chr2: 197,585,393-197,592,461 , GRCh37.p13 chr2: 198,450,117-198,457,185 RFTN2
    nsv6679934copy number variation1nstd229human GRCh38 chr2: 197,667,650-197,672,465 , GRCh37.p13 chr2: 198,532,374-198,537,189 RFTN2
    nsv6637127copy number variation1nstd102humanPathogenic GRCh37 chr2: 189,909,904-209,468,383 , GRCh38.p12 chr2: 189,045,178-208,603,658 LOC100421409, LOC100507443, 310 more genes
    nsv6636947copy number variation1nstd102humanUncertain significance GRCh37 chr2: 197,704,153-198,552,092 , GRCh38.p12 chr2: 196,839,429-197,687,368 SF3B1, RPL4P7, 17 more genes
    nsv6636571copy number variation1nstd102humanPathogenic GRCh37 chr2: 187,152,754-199,960,525 , GRCh38.p12 chr2: 186,288,027-199,095,802 GAPDHP59, OSGEPL1-AS1, 135 more genes
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