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Items: 1 to 20 of 205

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7054595inversion1nstd229human GRCh38 chr2: 129,115,794-130,999,381 , GRCh37.p13 chr2: 129,873,367-131,756,954 LOC646674, CYP4F27P, 65 more genes
    nsv7039305inversion1nstd229human GRCh38 chr2: 129,265,287-129,265,307 , GRCh37.p13 chr2: 130,022,860-130,022,880 LINC01854
    nsv6697853copy number variation1nstd229human GRCh38 chr2: 129,149,375-129,251,698 , GRCh37.p13 chr2: 129,906,948-130,009,271 LOC105373612, LINC01854
    nsv6689525copy number variation1nstd229human GRCh38 chr2: 128,477,084-129,647,405 , GRCh37.p13 chr2: 129,234,658-130,404,978 LOC105373613, LINC01854, 6 more genes
    nsv6689312copy number variation1nstd229human GRCh38 chr2: 129,008,741-129,269,365 , GRCh37.p13 chr2: 129,766,315-130,026,938 LINC01854, LOC105373612
    nsv6688816copy number variation1nstd229human GRCh38 chr2: 129,238,179-129,254,758 , GRCh37.p13 chr2: 129,995,752-130,012,331 LINC01854, LOC105373612
    nsv6688149copy number variation1nstd229human GRCh38 chr2: 129,258,691-129,266,049 , GRCh37.p13 chr2: 130,016,264-130,023,622 LINC01854
    nsv6687270copy number variation1nstd229human GRCh38 chr2: 129,247,936-129,249,935 , GRCh37.p13 chr2: 130,005,509-130,007,508 LOC105373612, LINC01854
    nsv6685046copy number variation1nstd229human GRCh38 chr2: 129,034,609-130,295,093 , GRCh37.p13 chr2: 129,792,182-131,052,666 NMTRQ-TTG7-1, MTATP6P7, 41 more genes
    nsv6679692copy number variation1nstd229human GRCh38 chr2: 128,625,642-138,426,614 , GRCh37.p13 chr2: 129,383,216-139,184,184 MTND4P27, LOC646674, 194 more genes
    nsv6536888inversion1nstd223human GRCh38 chr2: 129,115,769-130,999,356 , GRCh37.p13 chr2: 129,873,342-131,756,929 FAR2P2, ARHGEF4, 65 more genes
    nsv6355258copy number variation1nstd223human GRCh38 chr2: 129,238,179-129,254,753 , GRCh37.p13 chr2: 129,995,752-130,012,326 LOC105373612, LINC01854
    nsv6353290copy number variation1nstd223human GRCh38 chr2: 129,264,301-129,273,800 , GRCh37.p13 chr2: 130,021,874-130,031,373 LINC01854
    nsv6351484copy number variation1nstd223human GRCh38 chr2: 129,258,691-129,266,041 , GRCh37.p13 chr2: 130,016,264-130,023,614 LINC01854
    nsv6343109copy number variation1nstd223human GRCh38 chr2: 128,625,639-138,426,614 , GRCh37.p13 chr2: 129,383,213-139,184,184 CYP4F30P, CCDC74B, 194 more genes
    nsv6339153copy number variation1nstd223human GRCh38 chr2: 129,272,786-129,276,112 , GRCh37.p13 chr2: 130,030,359-130,033,685 LINC01854
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6314748copy number variation1nstd102humanPathogenic GRCh37 chr2: 112,475,655-145,691,999 , GRCh38.p12 chr2: 111,718,078-144,934,432 MED15P9, TMEM37, 474 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
    nsv6291353copy number variation1nstd102humanPathogenic GRCh37 chr2: 111,484,468-146,333,604 , GRCh38.p12 chr2: 110,726,891-145,576,036 LINC01120, LOC105373585, 490 more genes
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