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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4683194copy number variation1nstd102humanUncertain significance GRCh37 chr19: 52,249,175-52,263,162 , GRCh38.p12 chr19: 51,745,922-51,759,909 FPR2, FPR1
    nsv3904885copy number variation1nstd102humanPathogenic GRCh37 chr19: 68,029-59,110,290 , GRCh38.p12 chr19: 68,029-58,598,923 FPR2, ZNF321P, 2443 more genes
    nsv3903203copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,912-59,097,160 , GRCh38.p12 chr19: 260,912-58,585,793 FPR2, BABAM1, 2426 more genes
    nsv3903092copy number variation2nstd102humanPathogenic GRCh37 chr19: 260,912-58,956,888 , GRCh38.p12 chr19: 260,912-58,445,521 FPR2, LENG8, 2408 more genes
    nsv3919076copy number variation1nstd102humanPathogenic GRCh37 chr19: 48,432,832-59,083,573 , NCBI36 chr19: 53,124,644-63,775,385 , GRCh38 chr19: 47,929,575-58,572,206 FPR2, KCNA7, 697 more genes
    nsv3911950copy number variation1nstd102humanPathogenic GRCh37 chr19: 48,411,797-59,051,332 , NCBI36 chr19: 53,103,609-63,743,144 , GRCh38 chr19: 47,908,540-58,539,965 FPR2, LOC107987270, 694 more genes
    nsv4676357copy number variation1nstd102humanPathogenic GRCh37 chr19: 44,738,088-53,621,561 , GRCh38.p12 chr19: 44,233,935-53,118,308 FPR2, MIR4324, 485 more genes
    nsv3924732copy number variation1nstd102humanPathogenic GRCh38 chr19: 49,907,832-58,557,889 , GRCh37 chr19: 50,411,089-59,069,256 , NCBI36 chr19: 55,102,901-63,761,068 FPR2, RPL39P37, 556 more genes
    nsv4729755copy number variation1nstd102humanPathogenic GRCh37 chr19: 48,463,931-57,095,254 , GRCh38.p12 chr19: 47,960,674-56,583,886 FPR2, SIGLEC5, 574 more genes
    nsv3890862copy number variation1nstd102humanPathogenic GRCh37 chr19: 50,489,390-59,095,359 , GRCh38.p12 chr19: 49,986,133-58,583,992 FPR2, SIGLECL1, 552 more genes
    nsv3923909copy number variation1nstd102humanPathogenic NCBI36 chr19: 55,347,589-63,784,382 , GRCh37 chr19: 50,655,777-59,092,570 , GRCh38 chr19: 50,152,520-58,581,203 FPR2, OSCAR, 535 more genes
    nsv3891963copy number variation1nstd102humanPathogenic GRCh37 chr19: 50,740,074-59,097,160 , GRCh38.p12 chr19: 50,236,817-58,585,793 FPR2, RPS9, 535 more genes
    nsv3916611copy number variation1nstd102humanPathogenic GRCh37 chr19: 50,694,476-59,047,185 , NCBI36 chr19: 55,386,288-63,738,997 , GRCh38 chr19: 50,191,219-58,535,818 FPR2, RNU6-980P, 526 more genes
    nsv3922599copy number variation1nstd102humanPathogenic GRCh38 chr19: 51,141,518-58,539,965 , NCBI36 chr19: 56,336,587-63,743,144 , GRCh37 chr19: 51,644,775-59,051,332 FPR2, LOC100421130, 475 more genes
    nsv6313906copy number variation1nstd102humanLikely pathogenic GRCh37 chr19: 49,911,081-53,127,438 , GRCh38.p12 chr19: 49,407,824-52,624,185 FPR2, AP2A1, 212 more genes
    nsv3899491copy number variation1nstd102humanBenign GRCh37 chr19: 52,227,916-52,359,169 , GRCh38.p12 chr19: 51,724,663-51,855,916 FPR2, ZNF577, 4 more genes
    nsv3895116copy number variation1nstd102humanBenign GRCh37 chr19: 52,225,767-52,356,791 , GRCh38.p12 chr19: 51,722,514-51,853,538 FPR2, HAS1, 4 more genes
    nsv3897618copy number variation1nstd102humanBenign GRCh37 chr19: 52,224,551-52,328,897 , GRCh38.p12 chr19: 51,721,298-51,825,644 FPR2, ZNF577, 4 more genes
    nsv3906387copy number variation1nstd102humanBenign GRCh37 chr19: 52,273,226-52,631,600 , GRCh38.p12 chr19: 51,769,973-52,128,347 FPR2, ZNF432, 17 more genes
    nsv3910244copy number variation1nstd102humanBenign GRCh37 chr19: 52,272,356-52,627,403 , GRCh38 chr19: 51,769,103-52,124,150 , NCBI36 chr19: 56,964,168-57,319,215 FPR2, ZNF615, 17 more genes
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