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Items: 1 to 20 of 113

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137211copy number variation1nstd102humanPathogenic GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639 EXOC6, VCL, 1906 more genes
    nsv7137209copy number variation1nstd102humanPathogenic GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639 RNU7-12P, RNU1-65P, 1876 more genes
    nsv6887736copy number variation1nstd229human GRCh38 chr10: 73,803,840-73,817,042 , GRCh37.p13 chr10: 75,563,598-75,576,800 CAMK2G, NDST2
    nsv6881823copy number variation1nstd229human GRCh38 chr10: 73,809,884-73,821,682 , GRCh37.p13 chr10: 75,569,642-75,581,440 NDST2, CAMK2G
    nsv6437560copy number variation1nstd223human GRCh38 chr10: 73,673,561-73,872,094 , GRCh37.p13 chr10: 75,433,319-75,631,852 CAMK2G, FUT11, 12 more genes
    nsv6314185copy number variation1nstd102humanPathogenic GRCh37 chr10: 68,735,254-78,885,714 , GRCh38.p12 chr10: 66,975,496-77,125,956 SLC25A16, CTNNA3, 204 more genes
    nsv6132050copy number variation1nstd213human GRCh37 chr10: 75,330,000-75,750,001 , GRCh38.p12 chr10: 73,570,242-73,990,243 CAMK2G, GLUD1P3, 18 more genes
    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
    nsv5259208copy number variation1nstd204human GRCh37.p13 chr10: 75,539,845-75,573,415 , GRCh38.p13 chr10: 73,780,087-73,813,657 CAMK2G, NDST2, 4 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
    nsv4973771copy number variation1nstd200human GRCh38 chr10: 73,673,558-73,872,096 , GRCh37.p13 chr10: 75,433,316-75,631,854 FUT11, CAMK2G, 12 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
    nsv4601398copy number variation1nstd183human GRCh37 chr10: 75,571,209-75,571,272 , GRCh38.p12 chr10: 73,811,451-73,811,514 CAMK2G, NDST2
    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
    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
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