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Items: 1 to 20 of 130

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4903601copy number variation1nstd200human GRCh38 chr1: 69,426,370-69,527,516 , GRCh37.p13 chr1: 69,892,053-69,993,199 LOC105378789, LINC01758
    nsv4896156copy number variation1nstd200human GRCh38 chr1: 69,332,427-69,522,374 , GRCh37.p13 chr1: 69,798,110-69,988,057 LINC01758, LOC105378789
    nsv4888344inversion1nstd200human GRCh37 chr1: 51,769,169-94,478,994 , GRCh38.p12 chr1: 51,303,497-94,013,438 , ST13P20, 664 more genes
    nsv4783618copy number variation1nstd200human GRCh37 chr1: 69,798,110-69,988,057 , GRCh38.p12 chr1: 69,332,427-69,522,374 LOC105378789, LINC01758
    nsv4780923copy number variation1nstd200human GRCh37 chr1: 69,892,053-69,993,199 , GRCh38.p12 chr1: 69,426,370-69,527,516 LOC105378789, LINC01758
    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
    nsv4454000copy number variation1nstd102humanPathogenic GRCh37 chr1: 67,851,233-86,101,340 , GRCh38.p12 chr1: 67,385,550-85,635,657 NEXN, LOC107985391, 209 more genes
    nsv4453663copy number variation1nstd102humanPathogenic GRCh37 chr1: 59,922,631-72,058,653 , GRCh38.p12 chr1: 59,456,959-71,592,970 RNU6-387P, MIR3671, 170 more genes
    nsv4450384copy number variation1nstd102humannot provided GRCh37 chr1: 66,085,524-88,429,789 , GRCh38.p12 chr1: 65,619,841-87,964,106 DEPDC1, ERICH3-AS1, 264 more genes
    nsv4449847copy number variation1nstd102humanPathogenic GRCh37 chr1: 66,868,168-77,106,425 , GRCh38.p12 chr1: 66,402,485-76,640,740 GNG12-AS1, C1orf141, 118 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
    nsv4384169copy number variation1nstd173human GRCh37 chr1: 69,821,134-72,007,188 , GRCh38.p12 chr1: 69,355,451-71,541,505 , ANKRD13C, 27 more genes
    nsv4329469inversion1nstd166human GRCh37.p13 chr1: 67,732,337-71,589,227 , GRCh38.p12 chr1: 67,266,654-71,123,544 , GADD45A, 61 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
    nsv4048590copy number variation1nstd166human GRCh37.p13 chr1: 69,899,000-69,908,000 , GRCh38.p12 chr1: 69,433,317-69,442,317 LINC01758
    nsv4041716copy number variation1nstd166human GRCh37.p13 chr1: 69,884,500-69,911,400 , GRCh38.p12 chr1: 69,418,817-69,445,717 LINC01758
    nsv3909388copy number variation1nstd102humanPathogenic GRCh37 chr1: 57,816,246-71,791,607 , GRCh38 chr1: 57,350,574-71,325,924 , NCBI36 chr1: 57,588,834-71,564,195 RNU6-1031P, LOC107984963, 193 more genes
    nsv3908260copy number variation1nstd102humanPathogenic GRCh37 chr1: 67,330,808-77,589,066 , NCBI36 chr1: 67,103,396-77,361,654 , GRCh38 chr1: 66,865,125-77,123,381 RNA5SP50, LINC01360, 119 more genes
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