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Items: 1 to 20 of 394

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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
    nsv6117295copy number variation1nstd186human GRCh37 chrX: 100,172,738-100,172,836 , GRCh38.p12 chrX: 100,917,749-100,917,847 XKRX
    nsv6112690copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301 LOC105373176, ZFX-AS1, 2151 more genes
    nsv5884764copy number variation1nstd209human GRCh38 chrX: 100,897,222-100,927,176 , GRCh37.p13 chrX: 100,152,211-100,182,165 XKRX, NSA2P3
    nsv5880703copy number variation1nstd209human GRCh38 chrX: 100,917,748-100,917,846 , GRCh37.p13 chrX: 100,172,737-100,172,835 XKRX
    nsv5715687mobile element insertion1nstd211human GRCh38 chrX: 100,950,576-100,950,576 , GRCh37.p13 chrX: 100,205,565-100,205,565 XKRX
    nsv5669889copy number variation1nstd207human GRCh38 chrX: 100,917,748-100,917,846 , GRCh37.p13 chrX: 100,172,737-100,172,835 XKRX
    nsv5610074insertion1nstd207human GRCh38 chrX: 100,917,674-100,917,674 , GRCh37.p13 chrX: 100,172,663-100,172,663 XKRX
    nsv5557860mobile element insertion1nstd206human GRCh38 chrX: 100,950,576-100,950,627 , GRCh37.p13 chrX: 100,205,565-100,205,616 XKRX
    nsv5422559copy number variation1nstd206human GRCh38 chrX: 100,953,262-100,954,792 , GRCh37.p13 chrX: 100,208,251-100,209,781 CSGALNACT2P1, XKRX
    nsv5418023copy number variation1nstd206human GRCh38 chrX: 100,917,749-100,917,847 , GRCh37.p13 chrX: 100,172,738-100,172,836 XKRX
    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
    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
    nsv4905804copy number variation1nstd200human GRCh38 chrX: 100,363,871-100,949,127 , GRCh37.p13 chrX: 99,618,869-100,204,116 NSA2P3, SRPX2, 12 more genes
    nsv4893823copy number variation1nstd200human GRCh38 chrX: 100,901,929-100,911,155 , GRCh37.p13 chrX: 100,156,918-100,166,144 XKRX, NSA2P3
    nsv4893822copy number variation1nstd200human GRCh38 chrX: 100,891,664-100,894,000 , GRCh37.p13 chrX: 100,146,653-100,148,989 XKRX
    nsv4771990copy number variation1nstd200human GRCh37 chrX: 100,146,653-100,148,989 , GRCh38.p12 chrX: 100,891,664-100,894,000 XKRX
    nsv4769250copy number variation1nstd201human GRCh37 chrX: 96,096,220-155,208,244 , GRCh38.p12 chrX: 96,841,221-155,978,579 , AGTR2, 959 more genes
    nsv4769249copy number variation1nstd201human GRCh37 chrX: 61,728,816-155,233,846 , GRCh38.p12 chrX: 62,509,346-156,004,181 , ABCB7, 1364 more genes
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