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Items: 1 to 20 of 251

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5967739inversion1nstd209human GRCh38 chr10: 27,341,069-27,367,322 , GRCh37.p13 chr10: 27,629,998-27,656,251 FAM210CP, LINC02673
    nsv5921613copy number variation1nstd209human GRCh38 chr10: 27,314,818-27,417,440 , GRCh37.p13 chr10: 27,603,747-27,706,369 PTCHD3, FAM210CP, 5 more genes
    nsv5914682copy number variation1nstd209human GRCh38 chr10: 27,335,907-27,341,069 , GRCh37.p13 chr10: 27,624,836-27,629,998 LINC02673, RNU6-452P
    nsv5914382copy number variation1nstd209human GRCh38 chr10: 27,312,316-36,846,398 , GRCh37.p13 chr10: 27,601,245-37,135,326 , RN7SL241P, 160 more genes
    nsv5860628copy number variation1nstd209human GRCh38 chr10: 27,335,500-27,341,037 , GRCh37.p13 chr10: 27,624,429-27,629,966 ODAD2P1, LINC02673, 1 more genes
    nsv5859347copy number variation1nstd209human GRCh38 chr10: 27,334,512-27,341,062 , GRCh37.p13 chr10: 27,623,441-27,629,991 ODAD2P1, RNU6-452P, 1 more genes
    nsv5853323copy number variation1nstd209human GRCh38 chr10: 27,339,663-27,349,293 , GRCh37.p13 chr10: 27,628,592-27,638,222 FAM210CP, LINC02673
    nsv5712546mobile element insertion2nstd211human GRCh38 chr10: 27,344,910-27,344,910 , GRCh37.p13 chr10: 27,633,839-27,633,839 LINC02673
    nsv5591408copy number variation1nstd207human GRCh38 chr10: 27,335,920-27,341,069 , GRCh37.p13 chr10: 27,624,849-27,629,998 LINC02673, RNU6-452P
    nsv5561070sequence alteration1nstd206human GRCh38 chr10: 27,314,816-27,341,070 , GRCh37.p13 chr10: 27,603,745-27,629,999 ODAD2P1, LINC02673, 2 more genes
    nsv5492877copy number variation1nstd206human GRCh38 chr10: 27,314,819-27,417,441 , GRCh37.p13 chr10: 27,603,748-27,706,370 PTCHD3, FAM210CP, 5 more genes
    nsv5491638copy number variation1nstd206human GRCh38 chr10: 27,331,307-27,346,019 , GRCh37.p13 chr10: 27,620,236-27,634,948 ODAD2P1, RNU6-452P, 1 more genes
    nsv5490901copy number variation1nstd206human GRCh38 chr10: 27,335,512-27,341,070 , GRCh37.p13 chr10: 27,624,441-27,629,999 ODAD2P1, RNU6-452P, 1 more genes
    nsv5483050copy number variation1nstd206human GRCh38 chr10: 27,042,537-27,369,512 , GRCh37.p13 chr10: 27,331,466-27,658,441 RNU6-666P, ANKRD26, 12 more genes
    nsv5473925copy number variation1nstd206human GRCh38 chr10: 27,138,085-27,696,804 , GRCh37.p13 chr10: 27,427,014-27,985,733 TRIAP1P1, RNU2-24P, 15 more genes
    nsv5413379mobile element insertion1nstd206human GRCh38 chr10: 27,344,910-27,344,961 , GRCh37.p13 chr10: 27,633,839-27,633,890 LINC02673
    nsv5388311copy number variation1nstd186human GRCh37 chr10: 27,624,698-27,629,997 , GRCh38.p12 chr10: 27,335,769-27,341,068 , GRCh38.p12 chr10|NW_003315934.1: 97,415-102,714 LINC02673, RNU6-452P
    nsv5387428copy number variation1nstd186human GRCh37 chr10: 27,624,826-27,629,997 , GRCh38.p12 chr10: 27,335,897-27,341,068 , GRCh38.p12 chr10|NW_003315934.1: 97,543-102,714 LINC02673, RNU6-452P
    nsv5315732copy number variation1nstd204human GRCh38.p13 chr10: 27,314,797-27,417,461 , GRCh37.p13 chr10: 27,603,726-27,706,390 PTCHD3, FAM210CP, 5 more genes
    nsv5254958copy number variation1nstd204human GRCh38.p13 chr10: 27,334,001-27,343,100 , GRCh37.p13 chr10: 27,622,930-27,632,029 ODAD2P1, LINC02673, 1 more genes
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