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Items: 1 to 20 of 204

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7044475inversion1nstd229human GRCh38 chr2: 96,506,265-96,509,625 , GRCh37.p13 chr2: 97,172,002-97,175,362 NEURL3
    nsv6682476copy number variation1nstd229human GRCh38 chr2: 96,452,844-96,507,960 , GRCh37.p13 chr2: 97,118,581-97,173,697 NEURL3
    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
    nsv6543009inversion1nstd223human GRCh38 chr2: 96,490,094-96,496,738 , GRCh37.p13 chr2: 97,155,831-97,162,475 NEURL3
    nsv6338062copy number variation1nstd223human GRCh38 chr2: 96,490,094-96,496,905 , GRCh37.p13 chr2: 97,155,831-97,162,642 NEURL3
    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
    nsv6055943insertion1nstd212human GRCh38 chr2: 96,499,131-96,499,131 , GRCh37.p13 chr2: 97,164,868-97,164,868 NEURL3
    nsv5961185insertion1nstd209human GRCh38 chr2: 96,499,868-96,499,868 , GRCh37.p13 chr2: 97,165,605-97,165,605 NEURL3
    nsv5876678copy number variation1nstd209human GRCh38 chr2: 95,981,467-97,579,646 , GRCh37.p13 chr2: 96,647,215-98,196,109 , ARID5A, 48 more genes
    nsv5875852copy number variation1nstd209human GRCh38 chr2: 96,452,841-96,507,955 , GRCh37.p13 chr2: 97,118,578-97,173,692 NEURL3
    nsv5834213copy number variation1nstd209human GRCh38 chr2: 96,500,125-96,501,924 , GRCh37.p13 chr2: 97,165,862-97,167,661 NEURL3
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