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Items: 1 to 20 of 93

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5974464inversion1nstd209human GRCh38 chr19: 49,769,209-52,432,690 , GRCh37.p13 chr19: 50,272,466-52,935,943 , AP2A1, 172 more genes
    nsv5970571inversion1nstd209human GRCh38 chr19: 50,142,503-50,623,829 , GRCh37.p13 chr19: 50,645,760-51,127,086 KCNC3, MYBPC2, 16 more genes
    nsv5521879copy number variation1nstd206human GRCh38 chr19: 50,503,109-50,504,023 , GRCh37.p13 chr19: 51,006,366-51,007,280 JOSD2, EMC10
    nsv5322041copy number variation1nstd204human GRCh37.p13 chr19: 51,014,702-51,015,761 , GRCh38.p13 chr19: 50,511,445-50,512,504 JOSD2, ASPDH
    nsv5024823copy number variation1nstd200human GRCh38 chr19: 50,400,018-50,587,989 , GRCh37.p13 chr19: 50,903,275-51,091,246 LRRC4B, EMC10, 6 more genes
    nsv4865266copy number variation1nstd200human GRCh37 chr19: 50,903,275-51,091,246 , GRCh38.p12 chr19: 50,400,018-50,587,989 LRRC4B, JOSD2, 6 more genes
    nsv4853383copy number variation1nstd200human GRCh37 chr19: 51,014,732-51,015,741 , GRCh38.p12 chr19: 50,511,475-50,512,484 JOSD2, ASPDH
    nsv4853382copy number variation1nstd200human GRCh37 chr19: 51,006,500-51,007,363 , GRCh38.p12 chr19: 50,503,243-50,504,106 JOSD2, EMC10
    nsv4729755copy number variation1nstd102humanPathogenic GRCh37 chr19: 48,463,931-57,095,254 , GRCh38.p12 chr19: 47,960,674-56,583,886 SIGLEC5, MED25, 574 more genes
    nsv4685764copy number variation1nstd102humannot provided GRCh37 chr19: 47,939,842-54,626,871 , GRCh38.p12 chr19: 47,436,585-54,071,460 SNAR-G1, IRF3, 453 more genes
    nsv4676357copy number variation1nstd102humanPathogenic GRCh37 chr19: 44,738,088-53,621,561 , GRCh38.p12 chr19: 44,233,935-53,118,308 MIR4324, KLK9, 485 more genes
    nsv4676347copy number variation1nstd102humanUncertain significance GRCh37 chr19: 50,469,730-51,916,485 , GRCh38.p12 chr19: 49,966,473-51,413,231 VRK3, SYT3, 93 more genes
    nsv4457465copy number variation1nstd102humanUncertain significance GRCh37 chr19: 49,600,909-51,366,070 , GRCh38.p12 chr19: 49,097,652-50,862,814 MED25, EMC10, 117 more genes
    nsv4376838copy number variation1nstd173human GRCh37 chr19: 48,462,617-51,107,899 , GRCh38.p12 chr19: 47,959,360-50,604,642 , LIN7B, 173 more genes
    nsv4321864inversion1nstd166human GRCh37.p13 chr19: 46,657,897-51,634,775 , GRCh38.p12 chr19: 46,154,640-51,131,518 , C5AR1, 288 more genes
    nsv3962108insertion1nstd168human GRCh38 chr19: 50,489,353-50,508,583 , GRCh37.p13 chr19: 50,992,610-51,011,840 EMC10, JOSD2
    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 RPL39P37, CCDC106, 556 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 OSCAR, FKBP1AP1, 535 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 KCNA7, ZNF28, 697 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 RNU6-980P, ERVV-1, 526 more genes
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