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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6990864copy number variation1nstd229human GRCh38 chr17: 139,558-222,674 , GRCh37.p13 chr17|NW_004070872.2: 79,558-162,672 RPH3AL, LINC02091, 2 more genes
    nsv6206065copy number variation1nstd214human GRCh38 chr17: 139,325-139,430 , GRCh37.p13 chr17|NW_004070872.2: 79,325-79,430 SCGB1C2
    nsv6197382copy number variation1nstd214human GRCh38 chr17: 139,266-139,372 , GRCh37.p13 chr17|NW_004070872.2: 79,266-79,372 SCGB1C2
    nsv6196948copy number variation1nstd214human GRCh38 chr17: 130,944-131,032 , GRCh37.p13 chr17|NW_004070872.2: 70,944-71,032 SCGB1C2, LOC101929823
    nsv6189469copy number variation1nstd214human GRCh38 chr17: 139,278-139,490 , GRCh37.p13 chr17|NW_004070872.2: 79,278-79,490 SCGB1C2
    nsv6145050copy number variation1nstd206human GRCh38 chr17: 120,000-137,000 , GRCh37.p13 chr17|NW_004070872.2: 60,000-77,000 SCGB1C2, LOC101929823
    nsv6096948insertion1nstd212human GRCh38 chr17: 139,565-139,565 , GRCh37.p13 chr17|NW_004070872.2: 79,565-79,565 SCGB1C2
    nsv6089680insertion1nstd212human GRCh38 chr17: 139,496-139,496 , GRCh37.p13 chr17|NW_004070872.2: 79,496-79,496 SCGB1C2
    nsv6088476insertion1nstd212human GRCh38 chr17: 131,123-131,123 , GRCh37.p13 chr17|NW_004070872.2: 71,123-71,123 LOC101929823, SCGB1C2
    nsv6082706insertion1nstd212human GRCh38 chr17: 131,217-131,217 , GRCh37.p13 chr17|NW_004070872.2: 71,217-71,217 SCGB1C2, LOC101929823
    nsv6038240copy number variation1nstd212human GRCh38 chr17: 135,414-135,633 , GRCh37.p13 chr17|NW_004070872.2: 75,414-75,633 SCGB1C2
    nsv6032157copy number variation1nstd212human GRCh38 chr17: 139,410-139,620 , GRCh37.p13 chr17|NW_004070872.2: 79,410-79,620 SCGB1C2
    nsv6031701copy number variation1nstd212human GRCh38 chr17: 139,411-139,516 , GRCh37.p13 chr17|NW_004070872.2: 79,411-79,516 SCGB1C2
    nsv6031492copy number variation1nstd212human GRCh38 chr17: 139,292-139,398 , GRCh37.p13 chr17|NW_004070872.2: 79,292-79,398 SCGB1C2
    nsv6027788copy number variation1nstd212human GRCh38 chr17: 136,288-136,369 , GRCh37.p13 chr17|NW_004070872.2: 76,288-76,369 SCGB1C2
    nsv6022827copy number variation1nstd212human GRCh38 chr17: 134,608-134,665 , GRCh37.p13 chr17|NW_004070872.2: 74,608-74,665 SCGB1C2
    nsv5972750insertion1nstd209human GRCh38 chr17: 134,419-134,419 , GRCh37.p13 chr17|NW_004070872.2: 74,419-74,419 SCGB1C2
    nsv5933519copy number variation1nstd209human GRCh38 chr17: 134,604-134,664 , GRCh37.p13 chr17|NW_004070872.2: 74,604-74,664 SCGB1C2
    nsv5885283copy number variation1nstd209human GRCh38 chr17: 139,394-142,137 , GRCh37.p13 chr17|NW_004070872.2: 79,394-82,137 DOC2B, SCGB1C2
    nsv5665167inversion1nstd207human GRCh38 chr17: 10,002-139,264 , GRCh37.p13 chr17|NW_004070872.2: 1-79,264 SCGB1C2, LOC101929817, 5 more genes
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