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Items: 1 to 20 of 197

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5922354copy number variation1nstd209human GRCh38 chr7: 1,020,972-1,021,204 , GRCh37.p13 chr7: 1,060,608-1,060,840 MIR339, C7orf50
    nsv5911215copy number variation1nstd209human GRCh38 chr7: 930,402-2,311,664 , GRCh37.p13 chr7: 970,038-2,351,299 , GPR146, 40 more genes
    nsv5226601copy number variation1nstd204human GRCh38.p13 chr7: 909,101-1,222,900 , GRCh37.p13 chr7: 948,738-1,262,536 , ZFAND2A, 10 more genes
    nsv4729496copy number variation1nstd102humanUncertain significance GRCh37 chr7: 967,185-1,781,553 , GRCh38.p12 chr7: 927,549-1,741,917 ZFAND2A, LOC105375124, 25 more genes
    nsv4710679copy number variation1nstd195human GRCh37 chr7: 1,043,501-1,076,901 , GRCh38.p12 chr7: 1,003,865-1,037,265 C7orf50, MIR339
    nsv4675871copy number variation1nstd102humanPathogenic GRCh37 chr7: 44,935-1,750,797 , GRCh38.p12 chr7: 44,935-1,711,161 C7orf50, LOC105375123, 47 more genes
    nsv4675301copy number variation1nstd102humanPathogenic GRCh37 chr7: 43,360-1,648,288 , GRCh38.p12 chr7: 43,360-1,608,652 LOC112267991, MICALL2, 42 more genes
    nsv4456827copy number variation1nstd102humanPathogenic GRCh37 chr7: 43,376-19,520,619 , GRCh38.p12 chr7: 43,376-19,480,996 MIR6836, EEF1A1P26, 277 more genes
    nsv4456136copy number variation1nstd102humanPathogenic GRCh37 chr7: 36,616-4,298,168 , GRCh38.p12 chr7: 36,616-4,258,536 LOC442497, LFNG, 85 more genes
    nsv4455091copy number variation1nstd102humanPathogenic GRCh37 chr7: 10,365-159,119,707 , GRCh38.p12 chr7: 10,365-159,327,017 RPL23AP51, FLJ40288, 2684 more genes
    nsv4436745copy number variation1nstd102humanUncertain significance GRCh37 chr7: 869,147-1,438,686 , GRCh38.p12 chr7: 829,510-1,399,050 SUN1, GET4, 12 more genes
    nsv4403741copy number variation1nstd174human GRCh37 chr7: 863,281-1,114,300 , GRCh38.p12 chr7: 823,644-1,074,664 , MIR339, 8 more genes
    nsv4374613copy number variation1nstd173human GRCh37 chr7: 989,697-1,061,772 , GRCh38.p12 chr7: 950,061-1,022,136 C7orf50, COX19, 3 more genes
    nsv3923348copy number variation1nstd102humanPathogenic NCBI36 chr7: 149,268-6,644,183 , GRCh37 chr7: 54,185-6,677,658 , GRCh38 chr7: 54,185-6,638,027 ZNF890P, FOXK1, 143 more genes
    nsv3923236copy number variation1nstd102humanUncertain significance GRCh37 chr7: 54,185-1,370,682 , NCBI36 chr7: 149,268-1,337,208 , GRCh38 chr7: 54,185-1,331,046 PDGFA-DT, C7orf50, 33 more genes
    nsv3922360copy number variation1nstd102humanUncertain significance GRCh37 chr7: 729,191-2,071,156 , GRCh38 chr7: 689,554-2,031,521 , NCBI36 chr7: 695,717-2,037,682 LOC102723758, GET4, 32 more genes
    nsv3922329copy number variation1nstd102humanPathogenic GRCh37 chr7: 43,360-27,236,023 , GRCh38 chr7: 43,360-27,196,404 , NCBI36 chr7: 138,443-27,202,548 LOC401312, IQCE, 411 more genes
    nsv3922037copy number variation1nstd102humanBenign NCBI36 chr7: 902,439-1,028,542 , GRCh37 chr7: 935,913-1,062,016 , GRCh38 chr7: 896,276-1,022,380 ADAP1, MIR339, 4 more genes
    nsv3921351copy number variation1nstd102humanPathogenic GRCh37 chr7: 45,130-6,309,816 , GRCh38 chr7: 45,130-6,270,185 , NCBI36 chr7: 140,213-6,276,341 ELFN1, LINC02983, 131 more genes
    nsv3920006copy number variation1nstd102humanPathogenic GRCh37 chr7: 45,130-5,920,006 , GRCh38 chr7: 45,130-5,880,375 , NCBI36 chr7: 140,213-5,886,532 RNU6-215P, NUDT1, 120 more genes
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