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Items: 1 to 20 of 158

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098944copy number variation1nstd102humanUncertain significance GRCh37 chr19: 10,624,491-10,969,019 , GRCh38.p12 chr19: 10,513,815-10,858,343 DNM2, ILF3-DT, 17 more genes
    nsv7062606inversion1nstd229human GRCh38 chr19: 10,024,335-10,946,724 , GRCh37.p13 chr19: 10,135,011-11,057,400 FDX2, ICAM4, 48 more genes
    nsv7061047inversion1nstd229human GRCh38 chr19: 10,123,796-11,885,300 , GRCh37.p13 chr19: 10,234,472-11,996,115 QTRT1, ZNF653, 82 more genes
    nsv6998259copy number variation1nstd229human GRCh38 chr19: 10,046,601-11,033,768 , GRCh37.p13 chr19: 10,157,277-11,144,444 MRPL4, QTRT1, 49 more genes
    nsv6532250copy number variation1nstd223human GRCh38 chr19: 10,576,576-10,577,614 , GRCh37.p13 chr19: 10,687,252-10,688,290 AP1M2
    nsv6530340copy number variation1nstd223human GRCh38 chr19: 10,576,167-10,577,455 , GRCh37.p13 chr19: 10,686,843-10,688,131 AP1M2
    nsv6528360copy number variation1nstd223human GRCh38 chr19: 10,572,401-10,573,000 , GRCh37.p13 chr19: 10,683,077-10,683,676 AP1M2
    nsv6525989copy number variation1nstd223human GRCh38 chr19: 10,573,788-10,578,864 , GRCh37.p13 chr19: 10,684,464-10,689,540 AP1M2
    nsv6524136copy number variation1nstd223human GRCh38 chr19: 10,577,927-10,580,242 , GRCh37.p13 chr19: 10,688,603-10,690,918 AP1M2
    nsv6291543copy number variation1nstd102humanUncertain significance GRCh37 chr19: 9,941,033-11,739,567 , GRCh38.p12 chr19: 9,830,357-11,628,752 KRI1, SHFL, 88 more genes
    nsv6133698copy number variation1nstd213human GRCh37 chr19: 2,900,000-11,490,001 , GRCh38.p12 chr19: 2,900,002-11,379,325 , TLE5, 341 more genes
    nsv6133479copy number variation1nstd213human GRCh37 chr19: 7,400,000-13,280,001 , GRCh38.p12 chr19: 7,335,095-13,169,187 , ACP5, 299 more genes
    nsv6043574copy number variation1nstd212human GRCh38 chr19: 10,569,485-10,570,779 , GRCh37.p13 chr19: 10,680,161-10,681,455 AP1M2
    nsv5929215copy number variation1nstd209human GRCh38 chr19: 10,569,482-10,570,781 , GRCh37.p13 chr19: 10,680,158-10,681,457 AP1M2
    nsv5530963copy number variation1nstd206human GRCh38 chr19: 10,570,643-10,572,184 , GRCh37.p13 chr19: 10,681,319-10,682,860 AP1M2
    nsv5291380copy number variation1nstd204human GRCh38.p13 chr19: 10,335,201-10,670,200 , GRCh37.p13 chr19: 10,445,877-10,780,876 ICAM3, MIR1181, 15 more genes
    nsv5290904copy number variation1nstd204human GRCh38.p13 chr19: 10,584,601-10,647,700 , GRCh37.p13 chr19: 10,695,277-10,758,376 AP1M2, SLC44A2, 1 more genes
    nsv5287330copy number variation1nstd204human GRCh38.p13 chr19: 10,335,601-11,755,400 , GRCh37.p13 chr19: 10,446,277-11,866,215 AP1M2, C19orf38, 64 more genes
    nsv5283750copy number variation1nstd204human GRCh37.p13 chr19: 10,617,077-10,686,476 , GRCh38.p13 chr19: 10,506,401-10,575,800 CDKN2D, AP1M2, 5 more genes
    nsv5177988mobile element insertion1nstd203human GRCh38 chr19: 10,571,790-10,571,826 , GRCh37.p13 chr19: 10,682,466-10,682,502 AP1M2
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