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Items: 1 to 20 of 384

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098718copy number variation1nstd102humanUncertain significance GRCh37 chr19: 1,206,913-3,771,740 , GRCh38.p12 chr19: 1,206,914-3,771,742 GIPC3, GNG7, 117 more genes
    nsv7095297copy number variation1nstd102humanUncertain significance GRCh37 chr19: 589,946-5,696,788 , GRCh38.p12 chr19: 589,946-5,696,777 NCLN, RN7SL202P, 223 more genes
    nsv7095296copy number variation1nstd102humanUncertain significance GRCh37 chr19: 589,946-2,151,333 , GRCh38.p12 chr19: 589,946-2,151,334 ADAMTSL5, GPX4, 90 more genes
    nsv7095264copy number variation1nstd102humanPathogenic GRCh37 chr19: 1,206,913-1,650,247 , GRCh38.p12 chr19: 1,206,914-1,650,248 NDUFS7, GAMT, 30 more genes
    nsv7095226copy number variation1nstd102humanUncertain significance GRCh37 chr19: 589,946-4,818,389 , GRCh38.p12 chr19: 589,946-4,818,377 ATP5F1D, LOC102723798, 204 more genes
    nsv7009060copy number variation1nstd229human GRCh38 chr19: 1,233,932-1,233,985 , GRCh37.p13 chr19: 1,233,931-1,233,984 CBARP
    nsv7002820copy number variation1nstd229human GRCh38 chr19: 1,236,979-1,247,486 , GRCh37.p13 chr19: 1,236,978-1,247,485 CBARP, LOC102723811, 2 more genes
    nsv6637184copy number variation1nstd102humanPathogenic GRCh37 chr19: 1,205,244-1,479,188 , GRCh38.p12 chr19: 1,205,245-1,479,189 C19orf25, EFNA2, 19 more genes
    nsv6624629copy number variation1nstd224human GRCh37 chr19: 1,218,523-1,268,178 , GRCh38.p12 chr19: 1,218,524-1,268,179 ATP5F1D, CIRBP, 7 more genes
    nsv6315518copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,911-2,256,387 , GRCh38.p12 chr19: 260,911-2,256,388 LOC100420586, RPS15, 113 more genes
    nsv6315510copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,911-1,319,319 , GRCh38.p12 chr19: 260,911-1,319,320 LOC101928450, LOC105372235, 66 more genes
    nsv6315302copy number variation1nstd102humanLikely pathogenic GRCh37 chr19: 1,205,797-1,226,452 , GRCh38.p12 chr19: 1,205,798-1,226,453 STK11, CBARP
    nsv6307527copy number variation1nstd186human GRCh37 chr19: 1,033,799-1,267,999 , GRCh38.p12 chr19: 1,033,800-1,268,000 CIRBP, LOC102723811, 16 more genes
    nsv6306890copy number variation1nstd186human GRCh37 chr19: 1,237,999-1,243,999 , GRCh38.p12 chr19: 1,238,000-1,244,000 ATP5F1D, CBARP
    nsv6145904copy number variation1nstd206human GRCh38 chr19: 1,238,000-1,244,000 , GRCh37.p13 chr19: 1,237,999-1,243,999 CBARP, ATP5F1D
    nsv6145724copy number variation1nstd206human GRCh38 chr19: 1,033,800-1,268,000 , GRCh37.p13 chr19: 1,033,799-1,267,999 GPX4, CIRBP, 16 more genes
    nsv6137832copy number variation1nstd102humanLikely pathogenic GRCh37 chr19: 1,222,006-1,227,591 , GRCh38.p12 chr19: 1,222,007-1,227,592 STK11, CBARP
    nsv6133707copy number variation1nstd213human GRCh37 chr19: 560,000-1,700,001 , GRCh38.p12 chr19: 560,000-1,700,002 ATP5F1D, AZU1, 73 more genes
    nsv6133692copy number variation1nstd213human GRCh37 chr19: 180,000-2,200,001 , GRCh38.p12 chr19: 180,000-2,200,002 ATP5F1D, AZU1, 113 more genes
    nsv6102682inversion1nstd212human GRCh38 chr19: 871,904-2,377,665 , GRCh37.p13 chr19: 871,904-2,377,663 AMH, ATP5F1D, 83 more genes
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