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Items: 1 to 20 of 133

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5974232inversion1nstd209human GRCh38 chr1: 89,416,055-90,249,673 , GRCh37.p13 chr1: 89,881,614-90,715,231 , LRRC8B, 15 more genes
    nsv5423223copy number variation1nstd206human GRCh38 chr1: 89,283,835-89,856,917 , GRCh37.p13 chr1: 89,749,518-90,322,476 , LOC100421401, 13 more genes
    nsv5034251inversion1nstd200human GRCh38 chr1: 89,189,893-89,972,465 , GRCh37.p13 chr1: 89,655,576-90,438,024 , LOC729930, 18 more genes
    nsv4888344inversion1nstd200human GRCh37 chr1: 51,769,169-94,478,994 , GRCh38.p12 chr1: 51,303,497-94,013,438 , ST13P20, 664 more genes
    nsv4876996inversion1nstd200human GRCh37 chr1: 89,655,576-90,438,024 , GRCh38.p12 chr1: 89,189,893-89,972,465 , LOC107985744, 18 more genes
    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
    nsv4745469copy number variation1nstd199human GRCh37 chr1: 86,005,697-146,486,085 , GRCh38.p12 chr1: 85,540,014-149,528,945 , TAF13, 920 more genes
    nsv4451609copy number variation1nstd102humanUncertain significance GRCh37 chr1: 89,546,802-90,520,362 , GRCh38.p12 chr1: 89,081,119-90,054,804 GBP2, LRRC8C-DT, 25 more genes
    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
    nsv4369683copy number variation1nstd173human GRCh37 chr1: 90,025,881-90,212,497 , GRCh38.p12 chr1: 89,560,322-89,746,938 , LRRC8B, 4 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
    nsv4315042inversion1nstd166human GRCh37.p13 chr1: 89,684,818-91,735,543 , GRCh38.p12 chr1: 89,219,135-91,269,986 , LRRC8B, 34 more genes
    nsv4056763copy number variation1nstd166human GRCh37.p13 chr1: 89,499,441-90,107,441 , GRCh38.p12 chr1: 89,033,758-89,641,882 , PTGES3P1, 18 more genes
    nsv3898327copy number variation1nstd102humanPathogenic GRCh38 chr1: 83,457,325-104,273,917 , GRCh37 chr1: 83,923,008-104,816,539 , NCBI36 chr1: 83,695,596-104,618,062 LINC01773, LOC107985095, 322 more genes
    nsv3885743copy number variation1nstd102humanPathogenic GRCh37 chr1: 72,044,544-92,505,091 , GRCh38.p12 chr1: 71,578,861-92,039,534 ZNHIT6, CCN1, 257 more genes
    nsv3885206copy number variation1nstd102humanPathogenic GRCh37 chr1: 82,154-249,218,992 , GRCh38.p12 chr1: 82,154-248,924,793 , SNAP47, 4927 more genes
    nsv3884414copy number variation2nstd102humanPathogenic GRCh37 chr1: 849,467-249,224,684 , GRCh38.p12 chr1: 914,087-248,930,485 , RNU1-153P, 4887 more genes
    nsv3877365copy number variation1nstd102humanPathogenic GRCh37 chr1: 47,851-249,228,449 , GRCh38.p12 chr1: 47,851-248,934,250 , MARK1, 4930 more genes
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