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Items: 1 to 20 of 179

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5955860insertion1nstd209human GRCh38 chr1: 46,360,250-46,360,250 , GRCh37.p13 chr1: 46,825,922-46,825,922 NSUN4
    nsv5884477copy number variation1nstd209human GRCh38 chr1: 46,349,004-46,349,330 , GRCh37.p13 chr1: 46,814,676-46,815,002 NSUN4
    nsv5346057translocation1nstd200human GRCh38 chr1: 46,354,056-46,354,056 , GRCh38 chr1: 46,353,876-46,353,876 , GRCh37.p13 chr1: 46,819,548-46,819,548 , GRCh37.p13 chr1: 46,819,728-46,819,728 NSUN4
    nsv5286043copy number variation1nstd204human GRCh38.p13 chr1: 46,358,966-46,361,117 , GRCh37.p13 chr1: 46,824,638-46,826,789 NSUN4
    nsv5211256copy number variation1nstd204human GRCh38.p13 chr1: 46,358,960-46,361,464 , GRCh37.p13 chr1: 46,824,632-46,827,136 NSUN4
    nsv5205982mobile element deletion1nstd204human GRCh38.p13 chr1: 46,359,541-46,359,760 , GRCh37.p13 chr1: 46,825,213-46,825,432 NSUN4
    nsv5070816mobile element insertion1nstd203human GRCh38 chr1: 46,360,228-46,360,250 , GRCh37.p13 chr1: 46,825,900-46,825,922 NSUN4
    nsv4906343copy number variation1nstd200human GRCh38 chr1: 46,358,969-46,361,108 , GRCh37.p13 chr1: 46,824,641-46,826,780 NSUN4
    nsv4773396mobile element deletion1nstd200human GRCh37 chr1: 46,825,224-46,825,424 , GRCh38.p12 chr1: 46,359,552-46,359,752 NSUN4
    nsv4773395copy number variation1nstd200human GRCh37 chr1: 46,824,641-46,826,780 , GRCh38.p12 chr1: 46,358,969-46,361,108 NSUN4
    nsv4767860inversion1nstd199human GRCh37 chr1: 17,051,740-234,912,187 , GRCh38.p12 chr1: 16,725,245-234,776,440 , ABCA4, 4269 more genes
    nsv4761183inversion1nstd199human GRCh37 chr1: 16,884,570-145,374,569 , GRCh38.p12 chr1: 16,558,075-149,528,945 , ABCA4, 2341 more genes
    nsv4751400inversion1nstd199human GRCh37 chr1: 17,125,657-234,919,132 , GRCh38.p12 chr1: 16,799,162-234,783,385 , ABCA4, 4264 more genes
    nsv4674638copy number variation1nstd102humanUncertain significance GRCh37 chr1: 46,768,408-47,174,149 , GRCh38.p12 chr1: 46,302,736-46,708,477 UQCRH, MKNK1-AS1, 17 more genes
    nsv4674480copy number variation1nstd102humanUncertain significance GRCh37 chr1: 46,501,759-46,898,503 , GRCh38.p12 chr1: 46,036,087-46,432,831 LRRC41, TSPAN1, 12 more genes
    nsv4581845copy number variation1nstd183human GRCh37 chr1: 46,805,652-46,810,297 , GRCh38.p12 chr1: 46,339,980-46,344,625 NSUN4
    nsv4564982mobile element insertion1nstd166human GRCh37.p13 chr1: 46,830,358-46,830,358 , GRCh38.p12 chr1: 46,364,686-46,364,686 NSUN4
    nsv4436181copy number variation1nstd102humanUncertain significance GRCh37 chr1: 10,333,430-103,467,088 , GRCh38.p12 chr1: 10,273,372-103,001,532 LINC01776, IGSF21-AS1, 1853 more genes
    nsv4326932inversion1nstd166human GRCh37.p13 chr1: 35,173,490-93,458,530 , GRCh38.p12 chr1: 34,707,889-92,992,973 , ATP6V0B, 1069 more genes
    nsv4048730copy number variation1nstd166human GRCh37.p13 chr1: 46,803,347-46,804,046 , GRCh38.p12 chr1: 46,337,675-46,338,374 NSUN4
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