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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5529449copy number variation1nstd206human GRCh38 chr19: 10,111,992-10,112,181 , GRCh37.p13 chr19: 10,222,668-10,222,857 PPAN-P2RY11, P2RY11, 1 more genes
    nsv5284255copy number variation1nstd204human GRCh38.p13 chr19: 10,061,101-10,331,300 , GRCh37.p13 chr19: 10,171,777-10,441,976 ICAM1, ICAM4, 19 more genes
    nsv5282992copy number variation1nstd204human GRCh38.p13 chr19: 10,101,101-10,105,700 , GRCh37.p13 chr19: 10,211,777-10,216,376 PPAN, ANGPTL6, 2 more genes
    nsv5014498copy number variation1nstd200human GRCh38 chr19: 10,102,367-10,133,810 , GRCh37.p13 chr19: 10,213,043-10,244,486 SNORD105B, P2RY11, 6 more genes
    nsv5011585copy number variation1nstd200human GRCh38 chr19: 10,114,498-10,114,599 , GRCh37.p13 chr19: 10,225,174-10,225,275 EIF3G, P2RY11, 1 more genes
    nsv4864914copy number variation1nstd200human GRCh37 chr19: 10,213,043-10,244,486 , GRCh38.p12 chr19: 10,102,367-10,133,810 ANGPTL6, P2RY11, 6 more genes
    nsv4679505copy number variation1nstd189human GRCh37.p13 chr19: 9,903,732-10,322,986 , GRCh38.p12 chr19: 9,793,056-10,212,310 DNMT1, P2RY11, 18 more genes
    nsv4624262copy number variation1nstd183human GRCh37 chr19: 10,218,959-10,370,939 , GRCh38.p12 chr19: 10,108,283-10,260,263 EIF3G, MIR4322, 9 more genes
    nsv4375402copy number variation1nstd173human GRCh37 chr19: 9,970,367-10,250,655 , GRCh38.p12 chr19: 9,859,691-10,139,979 P2RY11, RDH8, 12 more genes
    nsv4264683copy number variation1nstd166human GRCh37.p13 chr19: 10,219,886-10,239,223 , GRCh38.p12 chr19: 10,109,210-10,128,547 PPAN-P2RY11, PPAN, 3 more genes
    nsv4258124copy number variation1nstd166human GRCh37.p13 chr19: 10,211,551-10,232,005 , GRCh38.p12 chr19: 10,100,875-10,121,329 P2RY11, EIF3G, 5 more genes
    nsv3920616copy number variation1nstd102humanLikely pathogenic NCBI36 chr19: 8,802,823-13,303,041 , GRCh37 chr19: 8,941,823-13,442,041 , GRCh38 chr19: 8,831,147-13,331,227 ACP5, GET3, 236 more genes
    nsv3912242copy number variation1nstd102humanPathogenic GRCh37 chr19: 9,846,119-11,338,677 , GRCh38 chr19: 9,735,443-11,228,001 , NCBI36 chr19: 9,707,119-11,199,677 PPAN, S1PR5, 68 more genes
    nsv3904885copy number variation1nstd102humanPathogenic GRCh37 chr19: 68,029-59,110,290 , GRCh38.p12 chr19: 68,029-58,598,923 ZNF321P, ZNF861P, 2443 more genes
    nsv3903203copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,912-59,097,160 , GRCh38.p12 chr19: 260,912-58,585,793 BABAM1, BEST2, 2426 more genes
    nsv3903092copy number variation2nstd102humanPathogenic GRCh37 chr19: 260,912-58,956,888 , GRCh38.p12 chr19: 260,912-58,445,521 LENG8, SYDE1, 2408 more genes
    nsv3898900copy number variation1nstd102humanPathogenic GRCh37 chr19: 9,678,768-14,853,426 , GRCh38.p12 chr19: 9,568,092-14,742,614 FBXL12, DCAF15, 253 more genes
    nsv3879018copy number variation1nstd102humanUncertain significance GRCh37 chr19: 10,132,458-10,230,550 , GRCh38.p12 chr19: 10,021,782-10,119,874 SNORD105B, P2RY11, 9 more genes
    nsv3167344copy number variation1nstd151human GRCh37 chr19: 10,220,304-10,221,547 , GRCh38.p12 chr19: 10,109,628-10,110,871 SNORD105B, PPAN-P2RY11, 2 more genes
    nsv3166981copy number variation1nstd151human GRCh37 chr19: 10,124,112-10,421,621 , GRCh38.p12 chr19: 10,013,436-10,310,945 ANGPTL6, EIF3G, 20 more genes
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