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Items: 1 to 20 of 117

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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
    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
    nsv6966677copy number variation1nstd229human GRCh38 chr15: 88,579,320-88,699,378 , GRCh37.p13 chr15: 89,122,551-89,242,609 ISG20, MIR7-2, 4 more genes
    nsv6965626copy number variation1nstd229human GRCh38 chr15: 88,583,948-88,674,249 , GRCh37.p13 chr15: 89,127,179-89,217,480 ISG20, MIR7-2, 4 more genes
    nsv6961937copy number variation1nstd229human GRCh38 chr15: 88,597,762-88,935,692 , GRCh37.p13 chr15: 89,140,993-89,478,923 MIR1179, MFGE8, 8 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
    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
    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
    nsv4729092copy number variation1nstd102humanPathogenic GRCh37 chr15: 86,962,053-102,531,392 , GRCh38.p12 chr15: 86,418,822-101,981,189 CHD2, MIR11181, 272 more genes
    nsv4675149copy number variation1nstd102humanPathogenic GRCh37 chr15: 87,189,245-102,429,112 , GRCh38.p12 chr15: 86,646,014-101,888,909 TTLL13, LINC00052, 264 more genes
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