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Items: 1 to 20 of 118

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5558800sequence alteration1nstd206human GRCh38 chr19: 47,770,668-47,777,294 , GRCh37.p13 chr19: 48,273,925-48,280,551 SELENOW
    nsv5515671copy number variation1nstd206human GRCh38 chr19: 47,771,888-47,812,938 , GRCh37.p13 chr19: 48,275,145-48,316,195 TPRX1, RPL23AP80, 1 more genes
    nsv5288647copy number variation1nstd204human GRCh38.p13 chr19: 47,782,441-47,836,747 , GRCh37.p13 chr19: 48,285,698-48,340,004 TPRX1, SELENOW, 2 more genes
    nsv5284126copy number variation1nstd204human GRCh38.p13 chr19: 47,780,491-47,783,190 , GRCh37.p13 chr19: 48,283,748-48,286,447 SELENOW
    nsv5024773copy number variation1nstd200human GRCh38 chr19: 47,771,846-47,812,970 , GRCh37.p13 chr19: 48,275,103-48,316,227 SELENOW, RPL23AP80, 1 more genes
    nsv4865233copy number variation1nstd200human GRCh37 chr19: 48,275,111-48,316,258 , GRCh38.p12 chr19: 47,771,854-47,813,001 TPRX1, SELENOW, 1 more genes
    nsv4853214copy number variation1nstd200human GRCh37 chr19: 48,281,121-48,289,683 , GRCh38.p12 chr19: 47,777,864-47,786,426 SELENOW
    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
    nsv4679541copy number variation1nstd189human GRCh37.p13 chr19: 48,085,948-48,392,233 , GRCh38.p12 chr19: 47,582,691-47,888,976 CRX, SELENOW, 10 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
    nsv4676184copy number variation1nstd102humanUncertain significance GRCh37 chr19: 48,043,102-48,402,210 , GRCh38.p12 chr19: 47,539,845-47,898,953 RPL23AP80, SULT2A1, 12 more genes
    nsv4625283copy number variation1nstd183human GRCh37 chr19: 48,214,990-48,290,706 , GRCh38.p12 chr19: 47,711,733-47,787,449 NOP53-AS1, SELENOW, 3 more genes
    nsv4620657copy number variation1nstd183human GRCh37 chr19: 48,278,835-48,312,827 , GRCh38.p12 chr19: 47,775,578-47,809,570 SELENOW, TPRX1, 1 more genes
    nsv4457853copy number variation1nstd102humanUncertain significance GRCh37 chr19: 48,119,589-49,595,956 , GRCh38.p12 chr19: 47,616,332-49,092,699 DHDH, GRIN2D, 94 more genes
    nsv4457372copy number variation1nstd102humanPathogenic GRCh37 chr19: 28,271,106-49,213,832 , GRCh38.p12 chr19: 27,780,198-48,710,575 ZNF461, LOC101927572, 735 more genes
    nsv4428461copy number variation1nstd174human GRCh37 chr19: 48,250,461-48,411,104 , GRCh38.p12 chr19: 47,747,204-47,907,847 RPL23AP80, SNAR-A12, 9 more genes
    nsv4350827copy number variation1nstd102humanPathogenic GRCh37 chr19: 47,036,361-48,525,536 , GRCh38.p12 chr19: 46,533,104-48,022,279 LINC01595, SNAR-A13, 59 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
    nsv4266466copy number variation1nstd166human GRCh37.p13 chr19: 48,280,477-48,296,725 , GRCh38.p12 chr19: 47,777,220-47,793,468 SELENOW, RPL23AP80
    nsv4266176copy number variation1nstd166human GRCh37.p13 chr19: 48,283,000-48,288,000 , GRCh38.p12 chr19: 47,779,743-47,784,743 SELENOW
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