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Items: 1 to 20 of 227

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6637051copy number variation1nstd102humanUncertain significance GRCh37 chr2: 96,628,608-96,981,369 , GRCh38.p12 chr2: 95,962,860-96,315,631 FAHD2CP, ASTL, 12 more genes
    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
    nsv6628428copy number variation1nstd224human GRCh37 chr2: 96,423,982-96,690,279 , GRCh38.p12 chr2: 95,758,234-96,024,531 LINC00342, GPAT2, 4 more genes
    nsv6628427copy number variation1nstd224human GRCh37 chr2: 96,378,210-96,690,279 , GRCh38.p12 chr2: 95,712,462-96,024,531 LINC00342, GPAT2, 4 more genes
    nsv6628240copy number variation1nstd224human GRCh37 chr2: 96,195,730-96,690,279 , GRCh38.p12 chr2: 95,529,982-96,024,531 OR7E102P, FAHD2CP, 13 more genes
    nsv6547092inversion1nstd223human GRCh38 chr2: 96,007,660-97,097,743 , GRCh37.p13 chr2: 96,673,408-97,763,480 CNNM4, DUSP2, 34 more genes
    nsv6348416copy number variation1nstd223human GRCh38 chr2: 96,005,501-96,009,100 , GRCh37.p13 chr2: 96,671,249-96,674,848 FAHD2CP
    nsv6348297copy number variation1nstd223human GRCh38 chr2: 96,000,101-96,008,900 , GRCh37.p13 chr2: 96,665,849-96,674,648 RN7SL210P, FAHD2CP
    nsv6344696copy number variation1nstd223human GRCh38 chr2: 96,006,801-96,009,200 , GRCh37.p13 chr2: 96,672,549-96,674,948 FAHD2CP
    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
    nsv6290784copy number variation1nstd102humanUncertain significance GRCh37 chr2: 96,544,603-98,025,634 , GRCh38.p12 chr2: 95,878,855-97,285,797 LOC100506076, FAHD2B, 39 more genes
    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
    nsv6104368inversion1nstd212human GRCh38 chr2: 95,752,382-96,071,259 , GRCh37.p13 chr2: 96,418,130-96,737,007 , LINC00342, 7 more genes
    nsv6103221inversion1nstd212human GRCh38 chr2: 95,946,252-97,156,223 , GRCh37.p13 chr2: 96,612,000-97,821,960 , ADRA2B, 39 more genes
    nsv5876678copy number variation1nstd209human GRCh38 chr2: 95,981,467-97,579,646 , GRCh37.p13 chr2: 96,647,215-98,196,109 , ARID5A, 48 more genes
    nsv5868663copy number variation1nstd209human GRCh38 chr2: 96,001,110-96,009,169 , GRCh37.p13 chr2: 96,666,858-96,674,917 RN7SL210P, FAHD2CP
    nsv5833530copy number variation1nstd209human GRCh38 chr2: 96,001,104-96,009,183 , GRCh37.p13 chr2: 96,666,852-96,674,931 FAHD2CP, RN7SL210P
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