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Items: 1 to 20 of 138

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148092copy number variation1nstd102humanPathogenic GRCh37 chr15: 75,165,490-102,520,892 , GRCh38.p12 chr15: 74,873,149-101,980,689 RPL9P8, COMMD4P1, 547 more genes
    nsv7098897copy number variation1nstd102humanPathogenic GRCh37 chr15: 67,358,491-91,644,328 , GRCh38.p12 chr15: 67,066,153-91,101,098 LINC00933, DNM1P9, 540 more genes
    nsv7098892copy number variation1nstd102humanPathogenic GRCh37 chr15: 84,228,005-102,264,590 , GRCh38.p12 chr15: 83,559,253-101,724,387 CIB1, RPS12P26, 326 more genes
    nsv7068128inversion1nstd229human GRCh38 chr15: 87,287,023-90,484,635 , GRCh37.p13 chr15: 87,830,254-91,027,867 , LOC105370964, 81 more genes
    nsv7062993inversion1nstd229human GRCh38 chr15: 85,570,479-90,463,746 , GRCh37.p13 chr15: 86,113,710-91,006,978 , NTRK3-AS1, 97 more genes
    nsv6976510copy number variation1nstd229human GRCh38 chr15: 86,730,503-91,149,191 , GRCh37.p13 chr15: 87,273,734-91,692,421 , IQGAP1, 105 more genes
    nsv6972964copy number variation1nstd229human GRCh38 chr15: 88,475,544-88,482,191 , GRCh37.p13 chr15: 89,018,775-89,025,422 MRPS11
    nsv6970400copy number variation1nstd229human GRCh38 chr15: 88,435,087-88,646,997 , GRCh37.p13 chr15: 88,978,318-89,190,228 MRPS11, MRPL46, 7 more genes
    nsv6637683copy number variation1nstd102humanPathogenic GRCh37 chr15: 77,512,817-102,035,027 , GRCh38.p12 chr15: 77,220,475-101,494,824 LINC02253, LOC107984790, 463 more genes
    nsv6582041inversion1nstd223human GRCh38 chr15: 85,570,476-90,463,749 , GRCh37.p13 chr15: 86,113,707-91,006,981 , AP3S2, 97 more genes
    nsv6501941copy number variation1nstd223human GRCh38 chr15: 88,475,555-88,482,168 , GRCh37.p13 chr15: 89,018,786-89,025,399 MRPS11
    nsv6290316copy number variation1nstd102humanPathogenic GRCh37 chr15: 88,465,861-94,411,846 , GRCh38.p12 chr15: 87,922,630-93,868,617 LOC105370964, MRPL46, 130 more genes
    nsv6133164copy number variation1nstd213human GRCh37 chr15: 88,260,000-89,240,001 , GRCh38.p12 chr15: 87,716,769-88,696,770 ISG20, AEN, 14 more genes
    nsv6133155copy number variation1nstd213human GRCh37 chr15: 72,730,000-102,440,001 , GRCh38.p12 chr15: 72,437,659-101,899,798 , BLM, 609 more genes
    nsv6132916copy number variation1nstd213human GRCh37 chr15: 84,950,000-91,460,001 , GRCh38.p12 chr15: 84,395,302-90,916,771 , FES, 147 more genes
    nsv6132827copy number variation1nstd213human GRCh37 chr15: 83,760,000-90,340,001 , GRCh38.p12 chr15: 83,091,248-89,796,770 , ANPEP, 136 more genes
    nsv6033226copy number variation1nstd212human GRCh38 chr15: 88,117,590-88,471,253 , GRCh37.p13 chr15: 88,660,821-89,014,484 NTRK3, MRPL46, 6 more genes
    nsv5529882copy number variation1nstd206human GRCh38 chr15: 88,475,544-88,482,191 , GRCh37.p13 chr15: 89,018,775-89,025,422 MRPS11
    nsv5380758copy number variation2nstd102humanUncertain significance GRCh37 chr15: 32,964,879-91,358,519 , GRCh38.p12 chr15: 32,672,678-90,815,289 LOC105370794, HNRNPA1P45, 1173 more genes
    nsv5009144copy number variation1nstd200human GRCh38 chr15: 88,475,545-88,482,191 , GRCh37.p13 chr15: 89,018,776-89,025,422 MRPS11
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