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Items: 1 to 20 of 161

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3879691copy number variation1nstd102humanBenign GRCh37 chr4: 1,003,890-1,006,924 , GRCh38.p12 chr4: 1,010,102-1,013,136 FGFRL1
    nsv3880016copy number variation1nstd102humanBenign GRCh37 chr4: 1,003,890-1,009,420 , GRCh38.p12 chr4: 1,010,102-1,015,632 FGFRL1
    nsv6311815copy number variation1nstd102humanUncertain significance GRCh37 chr4: 1,015,971-1,019,135 , GRCh38.p12 chr4: 1,022,183-1,025,347 FGFRL1
    nsv3871570copy number variation1nstd102humanBenign GRCh37 chr4: 947,035-1,019,312 , GRCh38.p12 chr4: 953,247-1,025,524 FGFRL1, SLC26A1, 3 more genes
    nsv3876082copy number variation1nstd102humanBenign GRCh37 chr4: 947,024-1,019,101 , GRCh38.p12 chr4: 953,236-1,025,313 FGFRL1, IDUA, 3 more genes
    nsv3882732copy number variation1nstd102humanBenign GRCh37 chr4: 947,035-1,019,101 , GRCh38.p12 chr4: 953,247-1,025,313 FGFRL1, SLC26A1, 3 more genes
    nsv3922676copy number variation1nstd102humanBenign/Likely benign NCBI36 chr4: 942,406-1,010,417 , GRCh38 chr4: 958,618-1,026,629 , GRCh37 chr4: 952,406-1,020,417 FGFRL1, DGKQ, 3 more genes
    nsv3918564copy number variation1nstd102humanBenign NCBI36 chr4: 942,465-1,010,417 , GRCh37 chr4: 952,465-1,020,417 , GRCh38 chr4: 958,677-1,026,629 FGFRL1, DGKQ, 3 more genes
    nsv3889162copy number variation1nstd102humanBenign GRCh37 chr4: 954,422-1,019,312 , GRCh38.p12 chr4: 960,634-1,025,524 FGFRL1, IDUA, 2 more genes
    nsv3875424copy number variation1nstd102humanBenign GRCh37 chr4: 954,449-1,019,312 , GRCh38.p12 chr4: 960,661-1,025,524 FGFRL1, IDUA, 2 more genes
    nsv3911405copy number variation1nstd102humanBenign GRCh38 chr4: 975,137-1,026,688 , GRCh37 chr4: 968,925-1,020,476 , NCBI36 chr4: 958,925-1,010,476 FGFRL1, SLC26A1, 1 more genes
    nsv3919324copy number variation1nstd102humanBenign/Likely benign GRCh38 chr4: 975,137-1,026,629 , NCBI36 chr4: 958,925-1,010,417 , GRCh37 chr4: 968,925-1,020,417 FGFRL1, SLC26A1, 1 more genes
    nsv3885762copy number variation1nstd102humanPathogenic GRCh37 chr4: 71,552-29,006,745 , GRCh38.p12 chr4: 71,660-29,005,123 FGFRL1, CD38, 456 more genes
    nsv3923296copy number variation1nstd102humanPathogenic GRCh38 chr4: 72,555-28,066,309 , NCBI36 chr4: 62,447-27,677,029 , GRCh37 chr4: 72,447-28,067,931 FGFRL1, OR7E99P, 446 more genes
    nsv4674378copy number variation1nstd102humanPathogenic GRCh37 chr4: 49,450-24,280,482 , GRCh38.p12 chr4: 49,556-24,278,859 FGFRL1, USP17L30, 394 more genes
    nsv6315347copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,345-20,964,575 , GRCh38.p12 chr4: 68,453-20,962,952 FGFRL1, LOC100421802, 375 more genes
    nsv6291097copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,345-20,587,167 , GRCh38.p12 chr4: 68,453-20,585,544 FGFRL1, LOC105374479, 372 more genes
    nsv3915161copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,345-20,387,231 , NCBI36 chr4: 58,345-19,996,329 , GRCh38 chr4: 68,453-20,385,608 FGFRL1, CTBP1-AS, 370 more genes
    nsv1398080copy number variation1nstd102humanPathogenic GRCh37 chr4: 44,020-19,796,182 , GRCh38.p12 chr4: 44,019-19,794,559 FGFRL1, RPL10AP7, 366 more genes
    nsv6112747copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,598-18,912,995 , GRCh38.p12 chr4: 68,706-18,911,372 FGFRL1, GPR78, 362 more genes
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