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Items: 1 to 20 of 277

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7048556inversion1nstd229human GRCh38 chr2: 100,298,284-100,306,746 , GRCh37.p13 chr2: 100,914,746-100,923,208 LONRF2
    nsv6696821copy number variation1nstd229human GRCh38 chr2: 100,106,299-100,276,473 , GRCh37.p13 chr2: 100,722,761-100,892,935 AFF3, LONRF2, 1 more genes
    nsv6695887copy number variation1nstd229human GRCh38 chr2: 99,662,903-100,342,170 , GRCh37.p13 chr2: 100,279,365-100,958,632 LOC105373504, LINC01104, 2 more genes
    nsv6688463copy number variation1nstd229human GRCh38 chr2: 100,314,494-100,340,952 , GRCh37.p13 chr2: 100,930,956-100,957,414 LONRF2
    nsv6683101copy number variation1nstd229human GRCh38 chr2: 100,111,642-100,877,626 , GRCh37.p13 chr2: 100,728,104-101,494,088 CHST10, CYCSP7, 16 more genes
    nsv6681432copy number variation1nstd229human GRCh38 chr2: 100,278,103-100,281,308 , GRCh37.p13 chr2: 100,894,565-100,897,770 LONRF2
    nsv6680100copy number variation1nstd229human GRCh38 chr2: 100,302,151-100,302,322 , GRCh37.p13 chr2: 100,918,613-100,918,784 LONRF2
    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
    nsv6353925copy number variation1nstd223human GRCh38 chr2: 100,322,301-100,327,200 , GRCh37.p13 chr2: 100,938,763-100,943,662 LONRF2
    nsv6343372copy number variation1nstd223human GRCh38 chr2: 100,318,101-100,321,500 , GRCh37.p13 chr2: 100,934,563-100,937,962 LONRF2
    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
    nsv6134229copy number variation1nstd213human GRCh37 chr2: 100,920,000-101,050,001 , GRCh38.p12 chr2: 100,303,538-100,433,539 CHST10, RALBP1P2, 2 more genes
    nsv5985149copy number variation1nstd212human GRCh38 chr2: 100,282,796-100,282,847 , GRCh37.p13 chr2: 100,899,258-100,899,309 LONRF2
    nsv5985074copy number variation1nstd212human GRCh38 chr2: 100,278,101-100,281,308 , GRCh37.p13 chr2: 100,894,563-100,897,770 LONRF2
    nsv5884885copy number variation1nstd209human GRCh38 chr2: 100,318,571-100,318,875 , GRCh37.p13 chr2: 100,935,033-100,935,337 LONRF2
    nsv5883526copy number variation1nstd209human GRCh38 chr2: 100,278,103-100,281,306 , GRCh37.p13 chr2: 100,894,565-100,897,768 LONRF2
    nsv5868873copy number variation1nstd209human GRCh38 chr2: 100,277,483-100,277,574 , GRCh37.p13 chr2: 100,893,945-100,894,036 LONRF2
    nsv5830866copy number variation1nstd209human GRCh38 chr2: 100,278,080-100,281,717 , GRCh37.p13 chr2: 100,894,542-100,898,179 LONRF2
    nsv5573417copy number variation1nstd207human GRCh38 chr2: 100,282,797-100,282,846 , GRCh37.p13 chr2: 100,899,259-100,899,308 LONRF2
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