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Items: 1 to 20 of 1623

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6120853copy number variation1nstd186human GRCh37 chr10: 46,654,811-46,665,141 , GRCh38.p12 chr10: 46,887,321-46,897,650 FRMPD2B
    nsv6112736copy number variation1nstd102humanPathogenic GRCh37 chr10: 48,301,535-51,807,296 , GRCh38.p12 chr10: 45,999,930-49,959,916 SHLD2P3, LOC100420617, 95 more genes
    nsv5947973insertion1nstd209human GRCh38 chr10: 46,876,545-46,876,545 , GRCh37.p13 chr10|NW_003871068.1: 1,147,660-1,147,660 FRMPD2B
    nsv5916113copy number variation1nstd209human GRCh38 chr10: 45,791,488-50,132,032 , GRCh37.p13 chr10|NW_003871068.1: 62,603-2,281,126 , GRCh37.p13 chr10: 46,591,857-51,891,792 , LINC02675, 111 more genes
    nsv5914502copy number variation1nstd209human GRCh38 chr10: 45,768,833-50,109,449 , GRCh37.p13 chr10: 46,591,857-51,028,871 , GRCh37.p13 chr10|NW_003871068.1: 39,948-2,281,126 , AGAP13P, 111 more genes
    nsv5910146copy number variation1nstd209human GRCh38 chr10: 46,108,417-47,381,921 , GRCh37.p13 chr10|NW_003871068.1: 379,532-1,653,036 , SYT15, 35 more genes
    nsv5856964copy number variation3nstd209human GRCh38 chr10: 46,868,871-46,879,951 , GRCh37.p13 chr10|NW_003871068.1: 1,139,986-1,151,066 FRMPD2B, LOC100420617
    nsv5694763mobile element insertion2nstd211human GRCh38 chr10: 46,876,556-46,876,556 , GRCh37.p13 chr10|NW_003871068.1: 1,147,671-1,147,671 FRMPD2B
    nsv5666496inversion1nstd207human GRCh38 chr10: 46,395,606-47,470,096 , GRCh37.p13 chr10|NW_003871068.1: 666,721-1,741,211 , GDF2, 29 more genes
    nsv5625088insertion1nstd207human GRCh38 chr10: 46,876,545-46,876,545 , GRCh37.p13 chr10|NW_003871068.1: 1,147,660-1,147,660 FRMPD2B
    nsv5492205copy number variation1nstd206human GRCh38 chr10: 46,888,265-46,894,265 , GRCh37.p13 chr10|NW_003871068.1: 1,159,380-1,165,380 FRMPD2B
    nsv5485699copy number variation1nstd206human GRCh38 chr10: 46,885,265-46,908,265 , GRCh37.p13 chr10|NW_003871068.1: 1,156,380-1,179,380 FRMPD2B
    nsv5480395copy number variation1nstd206human GRCh38 chr10: 46,714,265-46,880,265 , GRCh37.p13 chr10|NW_003871068.1: 985,380-1,151,380 BMS1P1, DUSP8P2, 8 more genes
    nsv5478354copy number variation1nstd206human GRCh38 chr10: 46,887,265-46,901,265 , GRCh37.p13 chr10|NW_003871068.1: 1,158,380-1,172,380 FRMPD2B
    nsv5475895copy number variation1nstd206human GRCh38 chr10: 46,886,265-46,906,265 , GRCh37.p13 chr10|NW_003871068.1: 1,157,380-1,177,380 FRMPD2B
    nsv5473969copy number variation1nstd206human GRCh38 chr10: 46,886,265-46,892,265 , GRCh37.p13 chr10|NW_003871068.1: 1,157,380-1,163,380 FRMPD2B
    nsv5406179mobile element insertion1nstd206human GRCh38 chr10: 46,876,545-46,876,545 , GRCh37.p13 chr10|NW_003871068.1: 1,147,660-1,147,660 FRMPD2B
    nsv5380941copy number variation1nstd102humanLikely pathogenic GRCh37 chr10: 49,033,586-52,417,694 , GRCh38.p12 chr10: 45,999,930-49,959,916 CHAT, CTSLP2, 95 more genes
    nsv5259501copy number variation1nstd204human GRCh38.p13 chr10: 46,888,910-46,893,844 , GRCh37.p13 chr10|NW_003871068.1: 1,160,025-1,164,959 FRMPD2B
    nsv5255351copy number variation1nstd204human GRCh38.p13 chr10: 46,868,701-46,880,100 , GRCh37.p13 chr10|NW_003871068.1: 1,139,816-1,151,215 FRMPD2B, LOC100420617
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