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Items: 1 to 20 of 163

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148117copy number variation1nstd102humanPathogenic GRCh37 chr10: 81,611,360-89,264,122 , GRCh38.p12 chr10: 79,851,604-87,504,365 ANXA11, FAM245A, 115 more genes
    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
    nsv6897907copy number variation1nstd229human GRCh38 chr10: 80,274,145-80,282,644 , GRCh37.p13 chr10: 82,033,901-82,042,400 MAT1A
    nsv6896866copy number variation1nstd229human GRCh38 chr10: 80,091,600-80,388,756 , GRCh37.p13 chr10: 81,851,356-82,148,512 LINC00857, EIF5AP4, 10 more genes
    nsv6895565copy number variation1nstd229human GRCh38 chr10: 80,283,752-80,283,823 , GRCh37.p13 chr10: 82,043,508-82,043,579 MAT1A
    nsv6894552copy number variation1nstd229human GRCh38 chr10: 80,287,609-80,287,805 , GRCh37.p13 chr10: 82,047,365-82,047,561 MAT1A
    nsv6893720copy number variation1nstd229human GRCh38 chr10: 76,896,077-84,570,412 , GRCh37.p13 chr10: 78,655,835-86,330,168 RNU6-129P, LOC105378392, 111 more genes
    nsv6888919copy number variation1nstd229human GRCh38 chr10: 80,179,318-80,273,713 , GRCh37.p13 chr10: 81,939,074-82,033,469 MAT1A, EIF5AP4, 4 more genes
    nsv6620535copy number variation1nstd224human GRCh37 chr10: 82,049,272-82,112,873 , GRCh38.p12 chr10: 80,289,516-80,353,117 MAT1A, ZNF519P1, 2 more genes
    nsv6585055inversion1nstd223human GRCh38 chr10: 79,754,380-87,461,415 , GRCh37.p13 chr10: 81,514,136-89,221,172 DYDC2, LOC105378394, 114 more genes
    nsv6315478copy number variation1nstd102humanPathogenic GRCh37 chr10: 81,630,468-88,980,961 , GRCh38.p12 chr10: 79,870,712-87,221,204 RNU1-19P, LOC107984187, 102 more genes
    nsv6291408copy number variation1nstd102humanUncertain significance GRCh37 chr10: 81,622,295-83,932,730 , GRCh38.p12 chr10: 79,862,539-82,172,974 LOC105378390, TMEM254-AS1, 34 more genes
    nsv6247286mobile element insertion1nstd215human GRCh38 chr10: 80,287,152-80,287,152 , GRCh37.p13 chr10: 82,046,908-82,046,908 MAT1A
    nsv6132054copy number variation1nstd213human GRCh37 chr10: 81,980,000-82,320,001 , GRCh38.p12 chr10: 80,220,244-80,560,245 MAT1A, TSPAN14, 8 more genes
    nsv5958563insertion1nstd209human GRCh38 chr10: 80,275,908-80,275,908 , GRCh37.p13 chr10: 82,035,664-82,035,664 MAT1A
    nsv5926561copy number variation1nstd209human GRCh38 chr10: 79,825,669-87,341,680 , GRCh37.p13 chr10: 81,585,425-89,101,437 , RPL12P29, 110 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
    nsv5475238copy number variation1nstd206human GRCh38 chr10: 80,279,740-80,279,820 , GRCh37.p13 chr10: 82,039,496-82,039,576 MAT1A
    nsv5030933inversion1nstd200human GRCh38 chr10: 57,233,666-95,028,660 , GRCh37.p13 chr10: 58,993,426-96,788,417 , RNU6-740P, 615 more genes
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