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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3895543copy number variation1nstd102humanBenign GRCh37 chr3: 1,797,444-2,026,210 , GRCh38 chr3: 1,755,760-1,984,526 , NCBI36 chr3: 1,772,444-2,001,210 RPL21P17
    nsv3877490copy number variation1nstd102humanBenign GRCh37 chr3: 1,820,234-1,982,410 , GRCh38.p12 chr3: 1,778,550-1,940,726 RPL21P17
    nsv3906169copy number variation1nstd102humanBenign GRCh38 chr3: 1,780,588-1,939,069 , NCBI36 chr3: 1,797,272-1,955,753 , GRCh37 chr3: 1,822,272-1,980,753 RPL21P17
    nsv3885314copy number variation1nstd102humanBenign GRCh37 chr3: 1,848,936-1,982,410 , GRCh38.p12 chr3: 1,807,252-1,940,726 RPL21P17
    nsv3889935copy number variation1nstd102humanLikely benign GRCh37 chr2: 36,461,440-36,529,829 , GRCh38.p12 chr2|NW_003315908.1: 66,663-135,052 , GRCh38.p12 chr2: 36,234,297-36,302,686 RPL21P36
    nsv3889154copy number variation1nstd102humanLikely benign GRCh37 chr2: 31,498,306-31,549,924 , GRCh38.p12 chr2: 31,275,440-31,327,058 RPL21P70
    nsv3892507copy number variation1nstd102humanBenign GRCh37 chr3: 1,922,459-1,962,679 , GRCh38 chr3: 1,880,775-1,920,995 , NCBI36 chr3: 1,897,459-1,937,679 RPL21P17
    nsv3908751copy number variation1nstd102humanLikely benign NCBI36 chr2: 31,351,810-31,403,428 , GRCh38 chr2: 31,275,440-31,327,058 , GRCh37 chr2: 31,498,306-31,549,924 RPL21P70
    nsv3882257copy number variation1nstd102humanBenign GRCh37 chr1: 48,946,572-48,967,002 , GRCh38.p12 chr1: 48,480,900-48,501,330 RPL21P25
    nsv3921449copy number variation1nstd102humanUncertain significance NCBI36 chr3: 1,772,472-1,982,897 , GRCh37.p13 chr3: 1,797,472-2,007,897 , GRCh38.p12 chr3: 1,755,788-1,966,213 RPL21P17
    nsv3924943copy number variation1nstd102humanUncertain significance NCBI36 chr3: 1,772,472-1,922,895 , GRCh37.p13 chr3: 1,797,472-1,947,895 , GRCh38.p12 chr3: 1,755,788-1,906,211 RPL21P17
    nsv3892974copy number variation1nstd102humanUncertain significance NCBI36 chr3: 1,797,272-2,062,270 , GRCh38 chr3: 1,780,588-2,045,586 , GRCh37 chr3: 1,822,272-2,087,270 RPL21P17
    nsv4682713copy number variation1nstd102humanPathogenic GRCh37 chr6: 10,556,637-10,626,860 , GRCh38.p12 chr6|NW_018654713.1: 67,288-137,511 , GRCh38.p12 chr6: 10,556,404-10,626,627 RPL21P63, GCNT2
    nsv7097170copy number variation1nstd102humanPathogenic GRCh37 chr6: 10,556,657-10,626,840 , GRCh38.p12 chr6|NW_018654713.1: 67,308-137,491 , GRCh38.p12 chr6: 10,556,424-10,626,607 RPL21P63, GCNT2
    nsv3881142copy number variation1nstd102humanPathogenic GRCh37 chr17: 41,197,694-41,267,742 , GRCh38 chr17: 43,045,677-43,115,725 BRCA1, RPL21P4
    nsv4683816copy number variation1nstd102humanPathogenic GRCh37 chr17: 41,197,675-41,258,570 , GRCh38.p12 chr17: 43,045,658-43,106,553 BRCA1, RPL21P4
    nsv3888055copy number variation1nstd102humanPathogenic GRCh37 chr17: 41,197,689-41,258,556 , GRCh38 chr17: 43,045,672-43,106,539 RPL21P4, BRCA1
    nsv3883854copy number variation1nstd102humanPathogenic GRCh38 chr17: 43,045,677-43,104,121 , GRCh37 chr17: 41,197,694-41,256,138 BRCA1, RPL21P4
    nsv3878731copy number variation1nstd102humanPathogenic GRCh38 chr17: 43,044,295-43,099,880 , GRCh37 chr17: 41,196,312-41,251,897 RPL21P4, BRCA1
    nsv4682869copy number variation1nstd102humanPathogenic GRCh37 chr17: 41,196,353-41,251,921 , GRCh38.p12 chr17: 43,044,336-43,099,904 BRCA1, RPL21P4
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