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Items: 1 to 20 of 104

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7075539inversion1nstd229human GRCh38 chr19: 48,377,786-50,073,353 , GRCh37.p13 chr19: 48,881,043-50,576,610 SNRNP70, PTOV1, 126 more genes
    nsv7074377inversion1nstd229human GRCh38 chr19: 41,965,396-49,981,454 , GRCh37.p13 chr19: 42,514,712-50,484,711 IGFL1, SYMPK, 400 more genes
    nsv7073220inversion1nstd229human GRCh38 chr19: 45,719,988-49,018,157 , GRCh37.p13 chr19: 46,223,246-49,521,414 RUVBL2, NTN5, 150 more genes
    nsv7064020inversion1nstd229human GRCh38 chr19: 48,004,601-50,148,757 , GRCh37.p13 chr19: 48,507,858-50,652,014 TEAD2, LHB, 155 more genes
    nsv7012452copy number variation1nstd229human GRCh38 chr19: 45,998,776-48,954,957 , GRCh37.p13 chr19: 46,502,034-49,458,214 TMEM160, SNORD23, 131 more genes
    nsv7005423copy number variation1nstd229human GRCh38 chr19: 48,632,328-48,632,455 , GRCh37.p13 chr19: 49,135,585-49,135,712 DBP
    nsv6598038inversion1nstd223human GRCh38 chr19: 45,719,988-49,018,154 , GRCh37.p13 chr19: 46,223,246-49,521,411 PLEKHA4, GAPDHP38, 150 more genes
    nsv6595834inversion1nstd223human GRCh38 chr19: 48,004,600-50,148,749 , GRCh37.p13 chr19: 48,507,857-50,652,006 KDELR1, VRK3, 155 more genes
    nsv6529545copy number variation1nstd223human GRCh38 chr19: 48,622,514-48,797,442 , GRCh37.p13 chr19: 49,125,771-49,300,699 BCAT2, SPHK2, 13 more genes
    nsv6209405copy number variation1nstd214human GRCh38 chr19: 48,632,328-48,632,454 , GRCh37.p13 chr19: 49,135,585-49,135,711 DBP
    nsv6133704copy number variation1nstd213human GRCh37 chr19: 45,030,000-55,230,001 , GRCh38.p12 chr19: 44,525,967-54,071,460 AP2A1, APOC1, 582 more genes
    nsv6133703copy number variation1nstd213human GRCh37 chr19: 41,220,000-49,640,001 , GRCh38.p12 chr19: 40,714,095-49,136,744 , APOC1, 402 more genes
    nsv6133474copy number variation1nstd213human GRCh37 chr19: 42,350,000-49,650,001 , GRCh38.p12 chr19: 41,845,937-49,146,744 , APOC1, 343 more genes
    nsv6110571inversion1nstd212human GRCh38 chr19: 47,903,487-50,091,196 , GRCh37.p13 chr19: 48,406,744-50,594,453 , AP2A1, 155 more genes
    nsv5929390copy number variation1nstd209human GRCh38 chr19: 48,632,328-48,632,454 , GRCh37.p13 chr19: 49,135,585-49,135,711 DBP
    nsv5667352inversion1nstd207human GRCh38 chr19: 47,959,661-50,091,195 , GRCh37.p13 chr19: 48,462,918-50,594,452 , AP2A1, 145 more genes
    nsv5533205copy number variation1nstd206human GRCh38 chr19: 48,632,357-48,632,455 , GRCh37.p13 chr19: 49,135,614-49,135,712 DBP
    nsv5380243translocation1nstd200human GRCh38 chr19: 843,261-843,261 , GRCh38 chr19: 48,631,180-48,631,180 , GRCh37.p13 chr19: 49,134,437-49,134,437 , GRCh37.p13 chr19: 843,261-843,261 PRTN3, DBP
    nsv5020924copy number variation1nstd200human GRCh38 chr19: 48,636,978-48,637,101 , GRCh37.p13 chr19: 49,140,235-49,140,358 SEC1P, DBP, 1 more genes
    nsv4730038copy number variation1nstd102humanLikely pathogenic GRCh37 chr19: 48,854,319-49,430,535 , GRCh38.p12 chr19: 48,351,062-48,927,278 BCAT2, CA11, 32 more genes
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