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Items: 1 to 20 of 151

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6636315copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 95,341,388-100,340,514 , GRCh38.p12 chr2: 94,675,663-99,724,052 ADRA2B, ATP5F1BP1, 130 more genes
    nsv6634330copy number variation1nstd102humanPathogenic GRCh37 chr2: 11,504,318-111,365,996 , GRCh38.p12 chr2: 11,364,192-110,608,419 CYP1B1-AS1, LOC107985771, 1649 more genes
    nsv6628239copy number variation1nstd224human GRCh37 chr2: 95,444,917-95,715,335 , GRCh38.p12 chr2: 94,779,172-95,049,590 MAL, RPS24P6, 9 more genes
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6314726copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 40,607,042-146,902,764 , GRCh38.p12 chr2: 40,379,902-146,145,196 ACTG2, ACYP2, 1713 more genes
    nsv6313735copy number variation1nstd102humanUncertain significance GRCh37 chr2: 95,341,387-96,735,978 , GRCh38.p12 chr2: 94,675,662-96,070,230 TRIM43, SNX18P14, 48 more genes
    nsv6291149copy number variation1nstd102humanUncertain significance GRCh37 chr2: 95,341,686-96,193,214 , GRCh38.p12 chr2: 94,675,961-95,527,466 CYP4F32P, UBTFL5, 32 more genes
    nsv6262569copy number variation1nstd214human GRCh38 chr2: 95,038,092-95,038,239 , GRCh37.p13 chr2: 95,703,837-95,703,984 MAL
    nsv6134374copy number variation1nstd213human GRCh37 chr2: 95,650,000-97,860,001 , GRCh38.p12 chr2: 94,984,255-97,194,264 ADRA2B, DUSP2, 68 more genes
    nsv6053272insertion1nstd212human GRCh38 chr2: 95,038,266-95,038,266 , GRCh37.p13 chr2: 95,704,011-95,704,011 MAL
    nsv6052417insertion1nstd212human GRCh38 chr2: 95,037,342-95,037,342 , GRCh37.p13 chr2: 95,703,087-95,703,087 MAL
    nsv5991132copy number variation1nstd212human GRCh38 chr2: 95,038,053-95,038,211 , GRCh37.p13 chr2: 95,703,798-95,703,956 MAL
    nsv5990656copy number variation1nstd212human GRCh38 chr2: 95,046,834-95,046,919 , GRCh37.p13 chr2: 95,712,579-95,712,664 MAL
    nsv5869283copy number variation1nstd209human GRCh38 chr2: 95,037,576-95,038,471 , GRCh37.p13 chr2: 95,703,321-95,704,216 MAL
    nsv5573518copy number variation1nstd207human GRCh38 chr2: 95,037,980-95,038,139 , GRCh37.p13 chr2: 95,703,725-95,703,884 MAL
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5035923inversion1nstd200human GRCh38 chr2: 83,726,586-172,391,178 , GRCh37.p13 chr2: 83,953,710-173,255,906 , MTND2P21, 1427 more genes
    nsv4908110copy number variation1nstd200human GRCh38 chr2: 95,040,594-95,041,665 , GRCh37.p13 chr2: 95,706,339-95,707,410 MAL
    nsv4908109copy number variation1nstd200human GRCh38 chr2: 95,037,167-95,039,153 , GRCh37.p13 chr2: 95,702,912-95,704,898 MAL
    nsv4777053copy number variation1nstd200human GRCh37 chr2: 95,702,912-95,704,898 , GRCh38.p12 chr2: 95,037,167-95,039,153 MAL
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