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Items: 1 to 20 of 148

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094683copy number variation1nstd102humanUncertain significance GRCh37 chr16: 65,821,800-72,146,396 , GRCh38.p12 chr16: 65,787,897-72,112,497 TRG-GCC5-1, RNU6-359P, 205 more genes
    nsv7075094inversion1nstd229human GRCh38 chr16: 67,913,190-69,541,641 , GRCh37.p13 chr16: 67,947,093-69,575,544 PSMB10, COG8, 52 more genes
    nsv7075084inversion1nstd229human GRCh38 chr16: 67,127,296-73,957,488 , GRCh37.p13 chr16: 67,161,199-73,991,387 MIR1538, LINC02136, 187 more genes
    nsv7058675inversion1nstd229human GRCh38 chr16: 67,667,666-75,720,241 , GRCh37.p13 chr16: 67,701,569-75,754,139 RNU6-898P, DPEP2, 199 more genes
    nsv6996038copy number variation1nstd229human GRCh38 chr16: 69,344,315-69,350,415 , GRCh37.p13 chr16: 69,378,218-69,384,318 TMED6
    nsv6994054copy number variation1nstd229human GRCh38 chr16: 69,342,155-69,347,525 , GRCh37.p13 chr16: 69,376,058-69,381,428 NIP7, TMED6
    nsv6992482copy number variation1nstd229human GRCh38 chr16: 69,350,573-69,352,643 , GRCh37.p13 chr16: 69,384,476-69,386,546 TMED6
    nsv6587581inversion1nstd223human GRCh38 chr16: 69,343,931-69,344,869 , GRCh37.p13 chr16: 69,377,834-69,378,772 TMED6
    nsv6507793copy number variation1nstd223human GRCh38 chr16: 69,342,155-69,347,522 , GRCh37.p13 chr16: 69,376,058-69,381,425 NIP7, TMED6
    nsv6506398copy number variation1nstd223human GRCh38 chr16: 69,344,489-69,344,751 , GRCh37.p13 chr16: 69,378,392-69,378,654 TMED6
    nsv6502259copy number variation1nstd223human GRCh38 chr16: 69,348,901-69,350,463 , GRCh37.p13 chr16: 69,382,804-69,384,366 TMED6
    nsv6315469copy number variation1nstd102humanPathogenic GRCh37 chr16: 68,971,067-74,823,560 , GRCh38.p12 chr16: 68,937,164-74,789,662 ZNF19, RNU7-71P, 128 more genes
    nsv6314755copy number variation1nstd102humanPathogenic GRCh37 chr16: 46,503,968-90,155,062 , GRCh38.p12 chr16: 46,470,056-90,088,654 ATMIN, ATP6V0D1, 826 more genes
    nsv6313976copy number variation1nstd102humanUncertain significance GRCh37 chr16: 68,850,677-69,377,553 , GRCh38.p12 chr16: 68,816,774-69,343,650 HAS3, LOC101060098, 17 more genes
    nsv6133200copy number variation1nstd213human GRCh37 chr16: 46,460,000-84,740,001 , GRCh38.p12 chr16: 46,426,088-84,706,395 , AARS1, 674 more genes
    nsv5943415copy number variation1nstd209human GRCh38 chr16: 69,345,210-69,346,689 , GRCh37.p13 chr16: 69,379,113-69,380,592 TMED6
    nsv5931374copy number variation1nstd209human GRCh38 chr16: 69,344,489-69,344,745 , GRCh37.p13 chr16: 69,378,392-69,378,648 TMED6
    nsv5877185copy number variation1nstd209human GRCh38 chr16: 69,345,682-69,347,031 , GRCh37.p13 chr16: 69,379,585-69,380,934 TMED6
    nsv5524354copy number variation1nstd206human GRCh38 chr16: 69,344,489-69,344,751 , GRCh37.p13 chr16: 69,378,392-69,378,654 TMED6
    nsv5522695copy number variation1nstd206human GRCh38 chr16: 69,341,321-69,341,531 , GRCh37.p13 chr16: 69,375,224-69,375,434 TMED6, NIP7
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