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Items: 1 to 20 of 108

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5471384copy number variation1nstd206human GRCh38 chr5: 26,833,978-43,674,414 , GRCh37.p13 chr5: 26,834,087-43,674,516 , INTS6P1, 221 more genes
    nsv5381781copy number variation1nstd102humanPathogenic GRCh37 chr5: 29,081,195-45,294,031 , GRCh38.p12 chr5: 29,081,088-45,293,929 ST3GAL5P1, LOC105374711, 213 more genes
    nsv5088132mobile element insertion1nstd203human GRCh38 chr5: 31,934,150-31,934,165 , GRCh37.p13 chr5: 31,934,256-31,934,271 MIR4279, PDZD2
    nsv5080258mobile element insertion1nstd203human GRCh38 chr5: 31,934,786-31,934,797 , GRCh37.p13 chr5: 31,934,892-31,934,903 PDZD2, MIR4279
    nsv4762598inversion1nstd199human GRCh37 chr5: 20,832,595-34,371,602 , GRCh38.p12 chr5: 20,832,486-34,371,497 , CDH6, 117 more genes
    nsv4751404inversion1nstd199human GRCh37 chr5: 20,834,824-34,371,606 , GRCh38.p12 chr5: 20,834,715-34,371,501 , CDH6, 117 more genes
    nsv4674644copy number variation1nstd102humanUncertain significance GRCh37 chr5: 29,720,391-34,124,081 , GRCh38.p12 chr5: 29,720,284-34,123,976 C1QTNF3, LOC105374703, 54 more genes
    nsv4591076copy number variation1nstd183human GRCh37 chr5: 31,895,052-32,128,346 , GRCh38.p12 chr5: 31,894,946-32,128,240 PDZD2, GOLPH3, 4 more genes
    nsv4436202copy number variation1nstd102humanUncertain significance GRCh37 chr5: 14,685,137-149,511,942 , GRCh38.p12 chr5: 14,685,028-150,132,379 RNU1-150P, RNU6-727P, 1757 more genes
    nsv4398696copy number variation1nstd174human GRCh37 chr5: 31,895,040-32,128,334 , GRCh38.p12 chr5: 31,894,934-32,128,228 PDZD2, GOLPH3, 4 more genes
    nsv4114167copy number variation1nstd166human GRCh37.p13 chr5: 31,935,325-31,936,149 , GRCh38.p12 chr5: 31,935,219-31,936,043 MIR4279, PDZD2
    nsv3924736copy number variation1nstd102humanPathogenic NCBI36 chr5: 75,149-33,454,051 , GRCh38 chr5: 22,149-33,418,188 , GRCh37 chr5: 22,149-33,418,294 LOC105374678, ZFR, 369 more genes
    nsv3924496copy number variation1nstd102humanPathogenic GRCh37 chr5: 22,149-32,248,116 , NCBI36 chr5: 75,149-32,283,873 , GRCh38 chr5: 22,149-32,248,010 LOC105374678, MIR4278, 356 more genes
    nsv3923992copy number variation1nstd102humanPathogenic GRCh37 chr5: 50,093-46,115,086 , NCBI36 chr5: 103,093-46,150,843 , GRCh38 chr5: 49,978-46,114,984 LOC100130748, CDH10, 533 more genes
    nsv3922539copy number variation1nstd102humanPathogenic NCBI36 chr5: 107,954-35,716,704 , GRCh37 chr5: 54,954-35,680,947 , GRCh38 chr5: 54,839-35,680,845 MTCYBP37, LINC01020, 398 more genes
    nsv3918728copy number variation1nstd102humanPathogenic GRCh38 chr5: 4,849,498-36,818,719 , NCBI36 chr5: 4,902,611-36,854,578 , GRCh37 chr5: 4,849,611-36,818,821 LINC02100, FTH1P10, 334 more genes
    nsv3916048copy number variation1nstd102humanUncertain significance NCBI36 chr5: 31,921,678-32,208,830 , GRCh37.p13 chr5: 31,885,921-32,173,073 , GRCh38.p12 chr5: 31,885,815-32,172,967 TPT1P5, LOC107986346, 4 more genes
    nsv3914649copy number variation1nstd102humanPathogenic GRCh38 chr5: 22,149-35,831,538 , GRCh37 chr5: 22,149-35,831,640 , NCBI36 chr5: 75,149-35,867,397 LOC105374666, CCNB3P1, 399 more genes
    nsv3914100copy number variation1nstd102humanPathogenic NCBI36 chr5: 30,184,899-35,249,537 , GRCh38 chr5: 30,149,035-35,213,678 , GRCh37 chr5: 30,149,142-35,213,780 GUSBP18, RXFP3, 61 more genes
    nsv3913699copy number variation1nstd102humanPathogenic GRCh37 chr5: 31,208,860-32,173,350 , NCBI36 chr5: 31,244,617-32,209,107 , GRCh38 chr5: 31,208,753-32,173,244 PDZD2, RPL21P56, 15 more genes
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