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Items: 1 to 20 of 208

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6681753copy number variation1nstd229human GRCh38 chr2: 96,108,701-96,114,000 , GRCh37.p13 chr2: 96,774,449-96,779,748 ADRA2B
    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
    nsv6628429copy number variation1nstd224human GRCh37 chr2: 96,747,466-98,186,298 , GRCh38.p12 chr2: 96,081,718-97,569,835 ARID5A, IGKV2OR2-2, 42 more genes
    nsv6628179copy number variation1nstd224human GRCh37 chr2: 96,721,808-98,186,298 , GRCh38.p12 chr2: 96,056,060-97,569,835 ADRA2B, IGKV2OR2-10, 43 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
    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
    nsv6311431copy number variation1nstd102humanUncertain significance GRCh37 chr2: 96,780,545-97,475,254 , GRCh38.p12 chr2: 96,114,797-96,809,517 LOC105373496, STARD7-AS1, 17 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
    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
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5381491copy number variation1nstd102humanPathogenic GRCh37 chr2: 96,755,045-98,021,592 , GRCh38.p12 chr2: 96,089,297-97,285,797 LOC100421288, STARD7, 34 more genes
    nsv5381324copy number variation1nstd102humanPathogenic GRCh37 chr2: 96,737,083-98,193,473 , GRCh38.p12 chr2: 96,071,335-97,577,010 IGKV2OR2-8, LOC100506076, 42 more genes
    nsv5215020copy number variation1nstd204human GRCh38.p13 chr2: 96,060,101-97,188,600 , GRCh37.p13 chr2: 96,725,849-97,854,337 RN7SL313P, NCAPH, 33 more genes
    nsv5035923inversion1nstd200human GRCh38 chr2: 83,726,586-172,391,178 , GRCh37.p13 chr2: 83,953,710-173,255,906 , MTND2P21, 1427 more genes
    nsv4766632inversion1nstd199human GRCh37 chr2: 87,997,505-112,010,501 , GRCh38.p12 chr1: 125,085,511-144,884,066 , GRCh38.p12 chr2: 87,697,986-111,252,924 , GRCh38.p12 chr9: 40,649,907-63,450,751 , GRCh38.p12 chr9: 40,649,751-63,450,622 , ADRA2B, 706 more genes
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