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Items: 1 to 20 of 664

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7142491insertion1nstd232human GRCh37.p13 chr8: 53,188,705-53,188,705 , GRCh38.p12 chr8: 52,276,145-52,276,145 ST18
    nsv7139702insertion1nstd232human GRCh37.p13 chr8: 53,236,442-53,236,442 , GRCh38.p12 chr8: 52,323,882-52,323,882 ST18
    nsv7078015inversion1nstd229human GRCh38 chr8: 52,231,118-52,231,177 , GRCh37.p13 chr8: 53,143,678-53,143,737 ST18
    nsv7074925inversion1nstd229human GRCh38 chr8: 52,387,110-52,748,740 , GRCh37.p13 chr8: 53,299,670-53,661,300 RB1CC1, ST18, 2 more genes
    nsv7074554inversion1nstd229human GRCh38 chr8: 51,106,732-53,057,419 , GRCh37.p13 chr8: 52,019,292-53,969,979 LOC105375835, RPL34P17, 14 more genes
    nsv7072507inversion1nstd229human GRCh38 chr8: 52,375,992-52,829,560 , GRCh37.p13 chr8: 53,288,552-53,742,120 ALKAL1, LOC105375835, 2 more genes
    nsv7067508inversion1nstd229human GRCh38 chr8: 51,755,366-56,976,322 , GRCh37.p13 chr8: 52,667,926-57,888,881 CHCHD2P10, LOC105375850, 81 more genes
    nsv6857335copy number variation1nstd229human GRCh38 chr8: 52,202,701-52,204,966 , GRCh37.p13 chr8: 53,115,261-53,117,526 ST18
    nsv6857158copy number variation1nstd229human GRCh38 chr8: 52,408,177-52,434,250 , GRCh37.p13 chr8: 53,320,737-53,346,810 ST18
    nsv6856883copy number variation1nstd229human GRCh38 chr8: 52,212,193-52,219,361 , GRCh37.p13 chr8: 53,124,753-53,131,921 ST18
    nsv6856214copy number variation1nstd229human GRCh38 chr8: 52,079,625-52,222,423 , GRCh37.p13 chr8: 52,992,185-53,134,983 ST18, LOC101929341
    nsv6853968copy number variation1nstd229human GRCh38 chr8: 52,122,868-52,122,940 , GRCh37.p13 chr8: 53,035,428-53,035,500 ST18
    nsv6852195copy number variation1nstd229human GRCh38 chr8: 52,312,235-52,316,113 , GRCh37.p13 chr8: 53,224,795-53,228,673 RPL34P17, ST18
    nsv6851455copy number variation1nstd229human GRCh38 chr8: 52,261,837-52,262,250 , GRCh37.p13 chr8: 53,174,397-53,174,810 ST18
    nsv6851218copy number variation1nstd229human GRCh38 chr8: 52,082,261-52,169,623 , GRCh37.p13 chr8: 52,994,821-53,082,183 ST18
    nsv6850454copy number variation1nstd229human GRCh38 chr8: 52,393,429-52,396,747 , GRCh37.p13 chr8: 53,305,989-53,309,307 ST18
    nsv6850180copy number variation1nstd229human GRCh38 chr8: 52,343,801-52,369,900 , GRCh37.p13 chr8: 53,256,361-53,282,460 ST18
    nsv6849941copy number variation1nstd229human GRCh38 chr8: 52,387,101-52,709,700 , GRCh37.p13 chr8: 53,299,661-53,622,260 ST18, ALKAL1, 1 more genes
    nsv6848158copy number variation1nstd229human GRCh38 chr8: 52,363,539-52,708,295 , GRCh37.p13 chr8: 53,276,099-53,620,855 ALKAL1, ST18, 1 more genes
    nsv6846576copy number variation1nstd229human GRCh38 chr8: 52,350,613-52,351,098 , GRCh37.p13 chr8: 53,263,173-53,263,658 ST18
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