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Items: 1 to 20 of 23

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4684263copy number variation4nstd102humanrisk factor, Benign GRCh37 chr5: 160,715,688-160,717,804 , GRCh38.p12 chr5: 161,288,681-161,290,797 GABRB2
    nsv4684268copy number variation4nstd102humanrisk factor, Benign GRCh37 chr5: 160,796,703-160,797,020 , GRCh38.p12 chr5: 161,369,697-161,370,014 GABRB2
    nsv3916072insertion7nstd102humanrisk factor, Pathogenic, Benign GRCh37 chr17: 61,565,892-61,565,892 , GRCh38 chr17: 63,488,531-63,488,531 ACE
    nsv6289947copy number variation1nstd102humanrisk factor GRCh37 chr9: 77,261,322-77,313,598 , GRCh38.p12 chr9: 74,646,406-74,698,682 RORB
    nsv6315064copy number variation1nstd102humanrisk factor GRCh37 chr21: 34,719,301-34,723,695 , GRCh38 chr21: 33,346,995-33,351,389 IFNAR1
    nsv6315032copy number variation1nstd102humanrisk factor GRCh38 chr21: 33,354,082-33,355,756 , GRCh37 chr21: 34,726,388-34,728,062 IFNAR1
    nsv6314771insertion1nstd102humanrisk factor GRCh37 chr11: 634,826-636,065 , GRCh38 chr11: 634,826-636,065 DRD4
    nsv3876319copy number variation2nstd102humanrisk factor, Pathogenic GRCh38 chr1: 196,753,076-196,839,375 , GRCh37 chr1: 196,722,206-196,808,505 CFHR1, CFHR3
    nsv3871638copy number variation2nstd102humanrisk factor, Pathogenic GRCh37 chr22: 18,893,735-18,924,066 , GRCh38 chr22: 18,906,222-18,936,553 PRODH, DGCR6
    nsv6634557copy number variation1nstd102humanrisk factor GRCh38 chr7: 83,833,300-84,046,323 , GRCh37.p13 chr7: 83,462,616-83,675,639 LOC107986745, SEMA3A
    nsv3889841copy number variation1nstd102humanrisk factor GRCh37.p13 chrX|NW_003871103.3: 2,958,612-3,046,770 , GRCh38 chrX: 155,524,633-155,612,791 , GRCh37.p13 chrX: 154,754,294-154,842,452 SPRY3, TMLHE
    nsv6137865copy number variation2nstd102humanrisk factor NCBI35 chr22: 27,408,285-27,462,376 , GRCh37.p13 chr22: 29,083,731-29,137,822 , GRCh38.p12 chr22: 28,687,743-28,741,834 CHEK2, HSCB
    nsv4578260copy number variation1nstd102humanrisk factor GRCh37 chr15: 32,157,104-32,418,879 , GRCh38.p12 chr15: 31,864,901-32,126,678 , GRCh38.p12 chr15|NT_187660.1: 4,150,040-4,411,820 , GRCh38.p12 chr15|NW_011332701.1: 4,037,588-4,299,368 CHRNA7, OTUD7A
    nsv6315094delins1nstd102humanrisk factor GRCh37 chr10: 124,216,821-124,217,264 , GRCh38 chr10: 122,457,305-122,457,748 ARMS2, LOC105378525
    nsv6137854copy number variation1nstd102humanrisk factor GRCh37 chrX: 5,168,397-5,925,195 , GRCh38.p12 chrX: 5,250,356-6,007,154 LINC03070, NLGN4X, 2 more genes
    nsv4768368copy number variation1nstd102humanrisk factor GRCh37 chr14: 66,881,928-67,493,801 , GRCh38.p12 chr14: 66,415,210-67,027,084 GPHN, CCDC196, 1 more genes
    nsv6290270copy number variation1nstd102humanrisk factor GRCh37 chr9: 119,311,659-119,462,832 , GRCh38.p12 chr9: 116,549,380-116,700,553 ASTN2, ASTN2-AS1, 3 more genes
    nsv5060037copy number variation1nstd102humanrisk factor GRCh37 chr16: 14,968,855-16,251,122 , GRCh38.p12 chr16: 14,874,998-16,157,265 , GRCh38.p12 chr16|NT_187607.1: 531,831-1,815,194 NPIPA5, MIR1972-1, 48 more genes
    nsv4685672copy number variation1nstd102humanrisk factor GRCh37 chr16: 29,446,604-30,218,886 , GRCh38.p12 chr16: 29,435,283-30,207,565 BOLA2-SMG1P6, HIRIP3, 53 more genes
    nsv6290204copy number variation1nstd102humanrisk factor GRCh37 chr1: 145,382,601-145,616,000 , GRCh38.p12 chr1: 145,819,092-146,052,399 ANKRD35, TRG-TCC2-1, 21 more genes
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