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Items: 1 to 20 of 436

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137666copy number variation1nstd102humanPathogenic GRCh37 chrX: 91,829,757-113,050,225 , GRCh38.p12 chrX: 92,574,758-113,806,943 TCEAL8, MTND5P26, 272 more genes
    nsv6112690copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301 LOC105373176, ZFX-AS1, 2151 more genes
    nsv5977263copy number variation1nstd209human GRCh38 chrX: 100,994,081-101,007,756 , GRCh37.p13 chrX: 100,249,070-100,262,745 TRMT2B
    nsv5885654copy number variation1nstd209human GRCh38 chrX: 100,998,704-101,006,536 , GRCh37.p13 chrX: 100,253,693-100,261,525 TRMT2B
    nsv5881818copy number variation1nstd209human GRCh38 chrX: 101,005,841-101,006,189 , GRCh37.p13 chrX: 100,260,830-100,261,178 TRMT2B
    nsv5877265copy number variation1nstd209human GRCh38 chrX: 101,046,675-101,046,979 , GRCh37.p13 chrX: 100,301,664-100,301,968 TRMT2B
    nsv5605754insertion2nstd207human GRCh38 chrX: 100,972,833-100,972,833 , GRCh37.p13 chrX: 100,227,822-100,227,822 ARL13A, TRMT2B
    nsv5605464insertion1nstd207human GRCh38 chrX: 100,972,874-100,972,874 , GRCh37.p13 chrX: 100,227,863-100,227,863 ARL13A, TRMT2B
    nsv5544857insertion1nstd206human GRCh38 chrX: 100,988,869-100,988,906 , GRCh37.p13 chrX: 100,243,858-100,243,895 TRMT2B, ARL13A
    nsv5421473copy number variation1nstd206human GRCh38 chrX: 101,049,341-101,049,618 , GRCh37.p13 chrX: 100,304,330-100,304,607 TRMT2B
    nsv5059979copy number variation1nstd102humanPathogenic GRCh37 chrX: 56,469,080-155,233,731 , GRCh38.p12 chrX: 56,442,647-156,004,066 VDAC1P1, LOC105373299, 1364 more genes
    nsv5030775inversion1nstd200human GRCh38 chrX: 23,472,124-121,561,941 , GRCh37.p13 chrX: 23,490,241-120,695,795 , GPR173, 1350 more genes
    nsv4905809copy number variation1nstd200human GRCh38 chrX: 101,046,959-101,049,563 , GRCh37.p13 chrX: 100,301,948-100,304,552 TRMT2B
    nsv4905808copy number variation1nstd200human GRCh38 chrX: 100,955,811-101,037,393 , GRCh37.p13 chrX: 100,210,800-100,292,382 ARL13A, TRMT2B, 2 more genes
    nsv4893824copy number variation1nstd200human GRCh38 chrX: 101,045,888-101,047,024 , GRCh37.p13 chrX: 100,300,877-100,302,013 TRMT2B
    nsv4771995copy number variation1nstd200human GRCh37 chrX: 100,301,754-100,305,530 , GRCh38.p12 chrX: 101,046,765-101,050,541 TRMT2B
    nsv4771994copy number variation1nstd200human GRCh37 chrX: 100,301,006-100,302,626 , GRCh38.p12 chrX: 101,046,017-101,047,637 TRMT2B
    nsv4771993copy number variation1nstd200human GRCh37 chrX: 100,298,029-100,304,249 , GRCh38.p12 chrX: 101,043,040-101,049,260 TRMT2B
    nsv4771992copy number variation1nstd200human GRCh37 chrX: 100,286,519-100,287,096 , GRCh38.p12 chrX: 101,031,530-101,032,107 TRMT2B
    nsv4771991copy number variation1nstd200human GRCh37 chrX: 100,277,830-100,281,264 , GRCh38.p12 chrX: 101,022,841-101,026,275 TRMT2B
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