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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5909992copy number variation1nstd209human GRCh38 chr10: 72,964,663-80,533,256 , GRCh37.p13 chr10: 74,724,421-82,293,012 , PRXL2A, 155 more genes
    nsv5301974copy number variation1nstd204human GRCh38.p13 chr10: 73,709,242-74,768,785 , GRCh37.p13 chr10: 75,469,000-76,528,543 , RPSAP6, 24 more genes
    nsv5250653copy number variation1nstd204human GRCh38.p13 chr10: 73,863,664-73,908,937 , GRCh37.p13 chr10: 75,623,422-75,668,695 CAMK2G, C10orf55, 1 more genes
    nsv5030933inversion1nstd200human GRCh38 chr10: 57,233,666-95,028,660 , GRCh37.p13 chr10: 58,993,426-96,788,417 , RNU6-740P, 615 more genes
    nsv4973772copy number variation1nstd200human GRCh38 chr10: 73,709,251-74,768,777 , GRCh37.p13 chr10: 75,469,009-76,528,535 , AP3M1, 24 more genes
    nsv4839922copy number variation1nstd200human GRCh37 chr10: 75,469,009-76,528,535 , GRCh38.p12 chr10: 73,709,251-74,768,777 , NDUFA8P1, 24 more genes
    nsv4456093copy number variation1nstd102humanUncertain significance GRCh37 chr10: 75,251,395-75,763,287 , GRCh38.p12 chr10: 73,491,637-74,003,529 ZSWIM8-AS1, PPP3CB-AS1, 23 more genes
    nsv4422261copy number variation1nstd174human GRCh37 chr10: 75,475,447-75,682,321 , GRCh38.p12 chr10: 73,715,689-73,922,563 GLUD1P3, ZSWIM8, 12 more genes
    nsv4343722sequence alteration1nstd166human GRCh37.p13 chr10: 43,905,894-92,001,956 , GRCh38.p12 chr10: 43,410,446-90,242,199 , ALOX5, 749 more genes
    nsv4339713sequence alteration1nstd166human GRCh37.p13 chr10: 8,718,069-114,609,729 , GRCh38.p12 chr10: 8,676,106-112,849,970 , ADRA2A, 1651 more genes
    nsv4189716copy number variation1nstd166human GRCh37.p13 chr10: 75,676,995-75,681,410 , GRCh38.p12 chr10: 73,917,237-73,921,652 PLAU, C10orf55
    nsv3924859copy number variation1nstd102humanPathogenic NCBI36 chr10: 52,159,133-88,896,941 , GRCh38 chr10: 50,729,367-87,147,204 , GRCh37 chr10: 52,489,127-88,906,961 BMS1P4-AGAP5, MTCO2P23, 471 more genes
    nsv3922335copy number variation1nstd102humanPathogenic GRCh37 chr10: 60,196,226-76,174,974 , GRCh38 chr10: 58,436,466-74,415,216 , NCBI36 chr10: 59,866,232-75,844,980 UNC5B-AS1, ALDH7A1P4, 250 more genes
    nsv3917966copy number variation1nstd102humanPathogenic NCBI36 chr10: 68,626,331-80,851,819 , GRCh37 chr10: 68,956,325-81,181,813 , GRCh38 chr10: 67,196,567-79,422,057 LINC02640, HK1, 231 more genes
    nsv3917822copy number variation1nstd102humanPathogenic GRCh38 chr10: 63,402,579-75,296,099 , GRCh37 chr10: 65,162,339-77,055,857 , NCBI36 chr10: 64,832,345-76,725,863 MYL6P3, CHCHD1, 220 more genes
    nsv3916110copy number variation1nstd102humanLikely benign GRCh38 chr10: 73,881,750-73,942,272 , GRCh37 chr10: 75,641,508-75,702,030 , NCBI36 chr10: 75,311,514-75,372,036 PLAU, C10orf55
    nsv3910545copy number variation1nstd102humanPathogenic NCBI36 chr10: 74,150,392-77,042,138 , GRCh38 chr10: 72,720,628-75,612,374 , GRCh37 chr10: 74,480,386-77,372,132 CAMK2G, MCU, 73 more genes
    nsv3907664copy number variation1nstd102humandrug response GRCh37 chr10: 42,347,406-135,534,747 , GRCh38.p12 chr10: 42,101,241-133,787,422 SHOC2, FAM245B, 1487 more genes
    nsv3906389copy number variation1nstd102humanPathogenic GRCh37 chr10: 73,232-135,524,321 , GRCh38.p12 chr10: 27,296-133,786,996 LOC100419870, LOC102724439, 2105 more genes
    nsv3905190copy number variation1nstd102humanPathogenic GRCh37 chr10: 75,542,067-79,428,995 , GRCh38.p12 chr10: 73,782,309-77,669,237 TIMM9P1, KCNMA1-AS2, 47 more genes
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