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Items: 1 to 20 of 122

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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
    nsv7075255inversion1nstd229human GRCh38 chr19: 49,270,356-54,089,823 , GRCh37.p13 chr19: 49,773,613-54,528,887 FPR2, SNAR-A11, 344 more genes
    nsv7075147inversion1nstd229human GRCh38 chr19: 49,467,064-49,473,885 , GRCh37.p13 chr19: 49,970,321-49,977,142 ALDH16A1, FLT3LG
    nsv7074377inversion1nstd229human GRCh38 chr19: 41,965,396-49,981,454 , GRCh37.p13 chr19: 42,514,712-50,484,711 IGFL1, SYMPK, 400 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
    nsv6595834inversion1nstd223human GRCh38 chr19: 48,004,600-50,148,749 , GRCh37.p13 chr19: 48,507,857-50,652,006 KDELR1, VRK3, 155 more genes
    nsv6532757copy number variation1nstd223human GRCh38 chr19: 49,479,228-49,479,535 , GRCh37.p13 chr19: 49,982,485-49,982,792 FLT3LG
    nsv6530240copy number variation1nstd223human GRCh38 chr19: 49,484,518-49,485,308 , GRCh37.p13 chr19: 49,987,775-49,988,565 FLT3LG
    nsv6313906copy number variation1nstd102humanLikely pathogenic GRCh37 chr19: 49,911,081-53,127,438 , GRCh38.p12 chr19: 49,407,824-52,624,185 AP2A1, KLK3, 212 more genes
    nsv6310544copy number variation1nstd102humanUncertain significance GRCh37 chr19: 49,519,325-50,366,015 , GRCh38.p12 chr19: 49,016,068-49,862,758 CGB5, MED25, 76 more genes
    nsv6146971copy number variation1nstd206human GRCh38 chr19: 49,446,874-49,481,000 , GRCh37.p13 chr19: 49,950,131-49,984,257 FLT3LG, PIH1D1, 1 more genes
    nsv6146446copy number variation1nstd206human GRCh38 chr19: 49,486,308-49,486,374 , GRCh37.p13 chr19: 49,989,565-49,989,631 RPL13A, FLT3LG
    nsv6133706copy number variation1nstd213human GRCh37 chr19: 49,520,000-50,090,001 , GRCh38.p12 chr19: 49,016,743-49,586,744 CD37, CGB3, 51 more genes
    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
    nsv6110571inversion1nstd212human GRCh38 chr19: 47,903,487-50,091,196 , GRCh37.p13 chr19: 48,406,744-50,594,453 , AP2A1, 155 more genes
    nsv6107957inversion1nstd212human GRCh38 chr19: 49,477,139-49,481,982 , GRCh37.p13 chr19: 49,980,396-49,985,239 FLT3LG
    nsv6053612copy number variation1nstd212human GRCh38 chr19: 49,481,891-49,482,320 , GRCh37.p13 chr19: 49,985,148-49,985,577 FLT3LG
    nsv5667352inversion1nstd207human GRCh38 chr19: 47,959,661-50,091,195 , GRCh37.p13 chr19: 48,462,918-50,594,452 , AP2A1, 145 more genes
    nsv5531469copy number variation1nstd206human GRCh38 chr19: 49,482,369-49,482,870 , GRCh37.p13 chr19: 49,985,626-49,986,127 FLT3LG
    nsv5530385copy number variation1nstd206human GRCh38 chr19: 49,487,226-49,493,412 , GRCh37.p13 chr19: 49,990,483-49,996,669 FLT3LG, RPL13A, 4 more genes
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