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Items: 1 to 20 of 172

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5949353insertion1nstd209human GRCh38 chr1: 67,409,420-67,409,420 , GRCh37.p13 chr1: 67,875,103-67,875,103 SERBP1
    nsv5884444copy number variation1nstd209human GRCh38 chr1: 67,423,052-67,423,344 , GRCh37.p13 chr1: 67,888,735-67,889,027 SERBP1
    nsv5419317copy number variation1nstd206human GRCh38 chr1: 67,416,635-67,416,688 , GRCh37.p13 chr1: 67,882,318-67,882,371 RNU6-387P, SERBP1
    nsv5352773translocation1nstd200human GRCh38 chr1: 67,397,792-67,397,792 , GRCh38 chr1: 67,407,742-67,407,742 , GRCh37.p13 chr1: 67,863,475-67,863,475 , GRCh37.p13 chr1: 67,873,425-67,873,425 SERBP1, IL12RB2
    nsv5068607mobile element insertion1nstd203human GRCh38 chr1: 67,424,020-67,424,028 , GRCh37.p13 chr1: 67,889,703-67,889,711 SERBP1
    nsv5068497mobile element insertion1nstd203human GRCh38 chr1: 67,425,520-67,425,537 , GRCh37.p13 chr1: 67,891,203-67,891,220 SERBP1
    nsv4888344inversion1nstd200human GRCh37 chr1: 51,769,169-94,478,994 , GRCh38.p12 chr1: 51,303,497-94,013,438 , ST13P20, 664 more genes
    nsv4783573copy number variation1nstd200human GRCh37 chr1: 67,863,475-67,873,425 , GRCh38.p12 chr1: 67,397,792-67,407,742 IL12RB2, SERBP1
    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
    nsv4673929copy number variation1nstd102humanUncertain significance GRCh37 chr1: 67,866,958-68,874,096 , GRCh38.p12 chr1: 67,401,275-68,408,413 SERBP1, HNRNPCP9, 20 more genes
    nsv4462241mobile element insertion1nstd166human GRCh37.p13 chr1: 67,891,203-67,891,203 , GRCh38.p12 chr1: 67,425,520-67,425,520 SERBP1
    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
    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
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