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Items: 1 to 20 of 249

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112797copy number variation1nstd102humanPathogenic GRCh37 chr16: 84,485-5,251,013 , GRCh38.p12 chr16: 34,485-5,201,012 ANTKMT, HBA1, 307 more genes
    nsv5946297copy number variation1nstd209human GRCh38 chr16: 2,471,842-2,471,895 , GRCh37.p13 chr16: 2,521,843-2,521,896 NTN3
    nsv5934013copy number variation1nstd209human GRCh38 chr16: 2,472,436-2,472,503 , GRCh37.p13 chr16: 2,522,437-2,522,504 NTN3
    nsv5520791copy number variation1nstd206human GRCh38 chr16: 2,472,436-2,472,513 , GRCh37.p13 chr16: 2,522,437-2,522,514 NTN3
    nsv5516299copy number variation1nstd206human GRCh38 chr16: 2,471,845-2,471,896 , GRCh37.p13 chr16: 2,521,846-2,521,897 NTN3
    nsv5380995copy number variation1nstd102humanUncertain significance GRCh37 chr16: 2,098,597-2,550,979 , GRCh38.p12 chr16: 2,048,596-2,500,978 TEDC2, MIR3677HG, 33 more genes
    nsv5349417translocation1nstd200human GRCh38 chr16: 2,472,513-2,472,513 , GRCh38 chr16: 2,472,436-2,472,436 , GRCh37.p13 chr16: 2,522,437-2,522,437 , GRCh37.p13 chr16: 2,522,514-2,522,514 NTN3
    nsv5335848translocation1nstd200human GRCh37 chr16: 2,522,514-2,522,514 , GRCh37 chr16: 2,522,437-2,522,437 , GRCh38.p12 chr16: 2,472,436-2,472,436 , GRCh38.p12 chr16: 2,472,513-2,472,513 NTN3
    nsv5311171copy number variation1nstd204human GRCh38.p13 chr16: 2,472,413-2,472,535 , GRCh37.p13 chr16: 2,522,414-2,522,536 NTN3
    nsv5271510copy number variation1nstd204human GRCh38.p13 chr16: 2,443,001-2,620,300 , GRCh37.p13 chr16: 2,493,002-2,670,301 LOC652276, PDPK1, 13 more genes
    nsv5269318copy number variation1nstd204human GRCh38.p13 chr16: 1,733,301-3,469,700 , GRCh37.p13 chr16: 1,783,302-3,519,700 , MIR6511B1, 156 more genes
    nsv5266471copy number variation1nstd204human GRCh38.p13 chr16: 1,936,501-2,552,200 , GRCh37.p13 chr16: 1,986,502-2,602,201 AMDHD2, MIR3178, 56 more genes
    nsv5265522copy number variation1nstd204human GRCh38.p13 chr16: 53,201-2,576,200 , GRCh37.p13 chr16: 103,201-2,626,201 , RHBDL1, 175 more genes
    nsv5007922copy number variation1nstd200human GRCh38 chr16: 2,471,262-2,471,526 , GRCh37.p13 chr16: 2,521,263-2,521,527 NTN3
    nsv5007921copy number variation1nstd200human GRCh38 chr16: 2,465,689-2,470,192 , GRCh37.p13 chr16: 2,515,690-2,520,193 TEDC2-AS1, NTN3
    nsv4866400copy number variation1nstd200human GRCh37 chr16: 2,515,690-2,520,193 , GRCh38.p12 chr16: 2,465,689-2,470,192 TEDC2-AS1, NTN3
    nsv4729241copy number variation1nstd102humanPathogenic GRCh37 chr16: 85,880-5,249,457 , GRCh38.p12 chr16: 35,880-5,199,456 MTRNR2L4, BRICD5, 307 more genes
    nsv4682518copy number variation1nstd102humanUncertain significance GRCh37 chr16: 624,055-2,550,979 , GRCh38.p12 chr16: 574,055-2,500,978 C1QTNF8, NHERF2, 133 more genes
    nsv4626841copy number variation1nstd183human GRCh37 chr16: 2,523,981-2,525,163 , GRCh38.p12 chr16: 2,473,980-2,475,162 NTN3, TBC1D24
    nsv4623151copy number variation1nstd183human GRCh37 chr16: 2,521,157-2,525,956 , GRCh38.p12 chr16: 2,471,156-2,475,955 TBC1D24, NTN3
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