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Items: 1 to 20 of 1361

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3910564copy number variation1nstd102humanLikely benign GRCh37 chr8: 10,059,525-10,112,371 , NCBI36 chr8: 10,096,935-10,149,781 , GRCh38 chr8: 10,202,015-10,254,861 MSRA
    nsv3918807copy number variation1nstd102humanLikely benign GRCh38 chr8: 10,095,976-10,148,214 , GRCh37 chr8: 9,953,486-10,005,724 , NCBI36 chr8: 9,990,896-10,043,134 MSRA
    nsv3903411copy number variation1nstd102humanBenign GRCh37 chr8: 9,975,212-10,026,131 , GRCh38.p12 chr8: 10,117,702-10,168,621 , GRCh38.p12 chr8|NW_018654717.1: 3,178,773-3,230,708 MSRA
    nsv4675971copy number variation1nstd102humanUncertain significance GRCh37 chr8: 9,987,099-10,120,304 , GRCh38.p12 chr8: 10,129,589-10,262,794 , GRCh38.p12 chr8|NW_018654717.1: 3,084,601-3,218,823 MSRA
    nsv6637130copy number variation1nstd102humanUncertain significance GRCh37 chr8: 10,014,085-10,079,045 , GRCh38.p12 chr8: 10,156,575-10,221,535 , GRCh38.p12 chr8|NW_018654717.1: 3,125,865-3,190,819 MSRA
    nsv510128sequence alteration3nstd49human NCBI35 chr8: 9,994,541-10,000,541 , GRCh37.p13 chr8: 9,957,131-9,963,131 , GRCh38.p12 chr8: 10,099,621-10,105,621 , GRCh38.p12 chr8|NW_018654717.1: 3,242,794-3,248,794 MSRA
    nsv6852804copy number variation1nstd229human GRCh38 chr8: 10,072,236-10,196,097 , GRCh37.p13 chr8: 9,929,746-10,053,607 MSRA
    nsv6852469copy number variation1nstd229human GRCh38 chr8: 10,060,552-10,182,572 , GRCh37.p13 chr8: 9,918,062-10,040,082 MSRA
    nsv6852631copy number variation1nstd229human GRCh38 chr8: 10,102,801-10,215,600 , GRCh37.p13 chr8: 9,960,311-10,073,110 MSRA
    nsv6838343copy number variation1nstd229human GRCh38 chr8: 9,940,188-10,047,720 , GRCh37.p13 chr8: 9,797,698-9,905,230 MSRA-DT
    nsv6856956copy number variation1nstd229human GRCh38 chr8: 10,131,160-10,237,532 , GRCh37.p13 chr8: 9,988,670-10,095,042 MSRA
    nsv6845769copy number variation1nstd229human GRCh38 chr8: 10,075,560-10,173,401 , GRCh37.p13 chr8: 9,933,070-10,030,911 MSRA
    nsv6846900copy number variation1nstd229human GRCh38 chr8: 10,241,154-10,322,886 , GRCh37.p13 chr8: 10,098,664-10,180,396 MSRA
    nsv6842359copy number variation1nstd229human GRCh38 chr8: 10,396,301-10,470,100 , GRCh37.p13 chr8: 10,253,811-10,327,610 MSRA
    nsv6846476copy number variation1nstd229human GRCh38 chr8: 10,086,225-10,157,824 , GRCh37.p13 chr8: 9,943,735-10,015,334 MSRA
    nsv6851497copy number variation1nstd229human GRCh38 chr8: 10,075,403-10,145,639 , GRCh37.p13 chr8: 9,932,913-10,003,149 MSRA
    nsv6856183copy number variation1nstd229human GRCh38 chr8: 9,987,768-10,047,818 , GRCh37.p13 chr8: 9,845,278-9,905,328 MSRA-DT
    nsv6855321copy number variation1nstd229human GRCh38 chr8: 10,339,964-10,393,447 , GRCh37.p13 chr8: 10,197,474-10,250,957 MSRA
    nsv6854023copy number variation1nstd229human GRCh38 chr8: 10,357,101-10,408,500 , GRCh37.p13 chr8: 10,214,611-10,266,010 MSRA
    nsv6856791copy number variation1nstd229human GRCh38 chr8: 10,182,397-10,227,517 , GRCh37.p13 chr8: 10,039,907-10,085,027 MSRA
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