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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3895769copy number variation1nstd102humanBenign GRCh37 chr10: 88,700,638-88,721,035 , GRCh38.p12 chr10: 86,940,881-86,961,278 MMRN2, SNCG
    nsv3903834copy number variation1nstd102humanBenign GRCh37 chr10: 88,700,638-88,718,833 , GRCh38.p12 chr10: 86,940,881-86,959,076 MMRN2, SNCG
    nsv3901429copy number variation1nstd102humanBenign GRCh37 chr10: 88,700,638-88,718,436 , GRCh38.p12 chr10: 86,940,881-86,958,679 MMRN2, SNCG
    nsv3894460copy number variation1nstd102humanBenign GRCh37 chr10: 88,702,230-88,719,789 , GRCh38.p12 chr10: 86,942,473-86,960,032 MMRN2, SNCG
    nsv3890869copy number variation1nstd102humanBenign GRCh37 chr10: 88,702,271-88,719,789 , GRCh38.p12 chr10: 86,942,514-86,960,032 MMRN2, SNCG
    nsv3899290copy number variation1nstd102humanBenign GRCh37 chr10: 88,702,230-88,718,436 , GRCh38.p12 chr10: 86,942,473-86,958,679 MMRN2, SNCG
    nsv3900121copy number variation1nstd102humanBenign GRCh37 chr10: 88,702,371-88,717,154 , GRCh38.p12 chr10: 86,942,614-86,957,397 MMRN2, SNCG
    nsv3907954copy number variation1nstd102humanBenign GRCh37 chr10: 88,702,371-88,713,604 , GRCh38.p12 chr10: 86,942,614-86,953,847 MMRN2, SNCG
    nsv3893667copy number variation1nstd102humanBenign GRCh37 chr10: 88,702,230-88,741,128 , GRCh38.p12 chr10: 86,942,473-86,981,371 MMRN2, ADIRF, 2 more genes
    nsv3893174copy number variation1nstd102humanBenign GRCh37 chr10: 88,702,271-88,741,128 , GRCh38.p12 chr10: 86,942,514-86,981,371 MMRN2, ADIRF, 2 more genes
    nsv3900971copy number variation1nstd102humanUncertain significance GRCh37 chr10: 88,581,181-88,711,003 , GRCh38.p12 chr10: 86,821,424-86,951,246 MMRN2, RNU1-19P, 2 more genes
    nsv6637329copy number variation1nstd102humanUncertain significance GRCh37 chr10: 88,580,250-88,708,342 , GRCh38.p12 chr10: 86,820,493-86,948,585 MMRN2, RNU1-19P, 2 more genes
    nsv6637227copy number variation1nstd102humanUncertain significance GRCh37 chr10: 88,581,433-88,708,342 , GRCh38.p12 chr10: 86,821,676-86,948,585 MMRN2, RNU1-19P, 2 more genes
    nsv3890537copy number variation1nstd102humanUncertain significance GRCh37 chr10: 88,584,364-88,711,004 , GRCh38.p12 chr10: 86,824,607-86,951,247 MMRN2, BMPR1A, 2 more genes
    nsv4675794copy number variation1nstd102humanUncertain significance GRCh37 chr10: 88,586,190-88,708,342 , GRCh38.p12 chr10: 86,826,433-86,948,585 MMRN2, RNU1-19P, 2 more genes
    nsv6290919copy number variation1nstd102humanUncertain significance GRCh37 chr10: 88,586,207-88,708,342 , GRCh38.p12 chr10: 86,826,450-86,948,585 MMRN2, RNU1-19P, 2 more genes
    nsv4681457copy number variation1nstd102humanPathogenic GRCh37 chr10: 88,428,449-88,713,917 , GRCh38.p12 chr10: 86,668,692-86,954,160 MMRN2, BMPR1A, 4 more genes
    nsv6309011copy number variation1nstd102humanPathogenic GRCh37 chr10: 88,441,193-88,722,432 , GRCh38.p12 chr10: 86,681,436-86,962,675 MMRN2, BMPR1A, 4 more genes
    nsv7137209copy number variation1nstd102humanPathogenic GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639 MMRN2, RNU7-12P, 1876 more genes
    nsv3920295copy number variation1nstd102humanPathogenic NCBI36 chr10: 81,675,342-135,374,737 , GRCh37.p13 chr10: 81,685,362-135,524,747 , GRCh38.p12 chr10: 79,925,606-133,787,422 MMRN2, EIF2S2P3, 895 more genes
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