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Items: 1 to 20 of 119

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095217copy number variation1nstd102humanUncertain significance GRCh37 chr19: 49,472,545-49,714,755 , GRCh38.p12 chr19: 48,969,288-49,211,498 NTF6A, CGB2, 25 more genes
    nsv7078081inversion1nstd229human GRCh38 chr19: 49,006,883-49,049,284 , GRCh37.p13 chr19: 49,510,140-49,552,541 CGB1, NTF6G, 14 more genes
    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
    nsv7073334inversion1nstd229human GRCh38 chr19: 48,958,315-49,037,642 , GRCh37.p13 chr19: 49,461,572-49,540,899 SNAR-G2, RUVBL2, 13 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
    nsv7063182inversion1nstd229human GRCh38 chr19: 49,028,832-49,040,076 , GRCh37.p13 chr19: 49,532,089-49,543,333 NTF6B, CGB1, 5 more genes
    nsv7062932inversion1nstd229human GRCh38 chr19: 49,028,645-49,040,076 , GRCh37.p13 chr19: 49,531,902-49,543,333 NTF6B, CGB1, 5 more genes
    nsv7010799copy number variation1nstd229human GRCh38 chr19: 49,027,801-49,045,400 , GRCh37.p13 chr19: 49,531,058-49,548,657 NTF6G, CGB5, 6 more genes
    nsv7009208copy number variation1nstd229human GRCh38 chr19: 49,032,284-49,044,258 , GRCh37.p13 chr19: 49,535,541-49,547,515 NTF6B, CGB1, 5 more genes
    nsv6999601copy number variation1nstd229human GRCh38 chr19: 49,016,212-49,036,276 , GRCh37.p13 chr19: 49,519,469-49,539,533 RUVBL2, NTF6B, 9 more genes
    nsv6599828inversion1nstd223human GRCh38 chr19: 49,028,839-49,039,986 , GRCh37.p13 chr19: 49,532,096-49,543,243 NTF6B, NTF6G, 4 more genes
    nsv6596715inversion1nstd223human GRCh38 chr19: 49,027,408-49,041,349 , GRCh37.p13 chr19: 49,530,665-49,544,606 NTF6B, NTF6G, 5 more genes
    nsv6596672inversion1nstd223human GRCh38 chr19: 49,027,654-49,041,129 , GRCh37.p13 chr19: 49,530,911-49,544,386 NTF6B, NTF6G, 5 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
    nsv6529802copy number variation1nstd223human GRCh38 chr19: 49,025,528-49,038,450 , GRCh37.p13 chr19: 49,528,785-49,541,707 NTF6A, NTF6B, 5 more genes
    nsv6526102copy number variation1nstd223human GRCh38 chr19: 49,020,102-49,058,451 , GRCh37.p13 chr19: 49,523,359-49,561,708 CGB3, CGB1, 12 more genes
    nsv6517027copy number variation1nstd223human GRCh38 chr19: 49,026,549-49,051,322 , GRCh37.p13 chr19: 49,529,806-49,554,579 LOC100287489, CGB5, 9 more genes
    nsv6516204copy number variation1nstd223human GRCh38 chr19: 49,026,337-49,045,771 , GRCh37.p13 chr19: 49,529,594-49,549,028 SNAR-G1, CGB5, 8 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
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