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Items: 1 to 20 of 98

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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
    nsv5940642copy number variation1nstd209human GRCh38 chr19: 50,996,430-50,996,492 , GRCh37.p13 chr19: 51,499,686-51,499,748 KLK8
    nsv5530691copy number variation1nstd206human GRCh38 chr19: 50,996,543-51,001,680 , GRCh37.p13 chr19: 51,499,799-51,504,936 KLK8, KLK9
    nsv5515287copy number variation1nstd206human GRCh38 chr19: 50,996,434-50,996,493 , GRCh37.p13 chr19: 51,499,690-51,499,749 KLK8
    nsv5359898translocation1nstd200human GRCh38 chr19: 51,001,324-51,001,324 , GRCh38 chr19: 51,001,872-51,001,872 , GRCh37.p13 chr19: 51,504,580-51,504,580 , GRCh37.p13 chr19: 51,505,128-51,505,128 KLK9, KLK8
    nsv5336062translocation1nstd200human GRCh37 chr19: 51,505,128-51,505,128 , GRCh37 chr19: 51,504,580-51,504,580 , GRCh38.p12 chr19: 51,001,324-51,001,324 , GRCh38.p12 chr19: 51,001,872-51,001,872 KLK9, KLK8
    nsv5327381copy number variation1nstd204human GRCh38.p13 chr19: 50,996,411-50,996,515 , GRCh37.p13 chr19: 51,499,667-51,499,771 KLK8
    nsv5024835copy number variation1nstd200human GRCh38 chr19: 50,983,236-51,013,588 , GRCh37.p13 chr19: 51,486,492-51,516,844 KLK7, KLK8, 2 more genes
    nsv5024833copy number variation1nstd200human GRCh38 chr19: 50,948,824-51,065,442 , GRCh37.p13 chr19: 51,452,080-51,568,699 , KLK11, 9 more genes
    nsv5021086copy number variation1nstd200human GRCh38 chr19: 51,000,915-51,004,433 , GRCh37.p13 chr19: 51,504,171-51,507,689 KLK9, KLK8
    nsv5021085copy number variation1nstd200human GRCh38 chr19: 50,996,543-51,001,680 , GRCh37.p13 chr19: 51,499,799-51,504,936 KLK8, KLK9
    nsv4865271copy number variation1nstd200human GRCh37 chr19: 51,452,080-51,568,699 , GRCh38.p12 chr19: 50,948,824-51,065,442 , KLK12, 9 more genes
    nsv4853418copy number variation1nstd200human GRCh37 chr19: 51,499,799-51,504,936 , GRCh38.p12 chr19: 50,996,543-51,001,680 KLK8, KLK9
    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
    nsv4634048copy number variation1nstd183human GRCh37 chr19: 51,409,215-51,497,644 , GRCh38.p12 chr19: 50,905,959-50,994,388 KLK7, KLK6, 5 more genes
    nsv4368703copy number variation1nstd173human GRCh37 chr19: 51,444,294-51,524,667 , GRCh38.p12 chr19: 50,941,038-51,021,411 KLK7, KLK6, 6 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
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