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Items: 1 to 20 of 215

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5919078copy number variation1nstd209human GRCh38 chr10: 8,050,504-8,050,554 , GRCh37.p13 chr10: 8,092,467-8,092,517 GATA3, GATA3-AS1
    nsv5488258copy number variation1nstd206human GRCh38 chr10: 8,058,984-8,059,039 , GRCh37.p13 chr10: 8,100,947-8,101,002 GATA3
    nsv5487071copy number variation1nstd206human GRCh38 chr10: 8,062,522-8,062,582 , GRCh37.p13 chr10: 8,104,485-8,104,545 GATA3
    nsv5483665copy number variation1nstd206human GRCh38 chr10: 8,068,271-8,069,386 , GRCh37.p13 chr10: 8,110,234-8,111,349 GATA3
    nsv5364734translocation1nstd200human GRCh38 chr10: 7,621,519-7,621,519 , GRCh38 chr10: 8,049,412-8,049,412 , GRCh37.p13 chr10: 8,091,375-8,091,375 , GRCh37.p13 chr10: 7,663,482-7,663,482 GATA3, ITIH5, 1 more genes
    nsv5333902translocation1nstd200human GRCh37 chr10: 8,091,375-8,091,375 , GRCh37 chr10: 7,663,482-7,663,482 , GRCh38.p12 chr10: 7,621,519-7,621,519 , GRCh38.p12 chr10: 8,049,412-8,049,412 GATA3, ITIH5, 1 more genes
    nsv5331816translocation1nstd200human GRCh37 chr10: 8,092,468-8,092,468 , GRCh37 chr10: 8,092,518-8,092,518 , GRCh38.p12 chr10: 8,050,505-8,050,505 , GRCh38.p12 chr10: 8,050,555-8,050,555 GATA3-AS1, GATA3
    nsv5133921mobile element insertion1nstd203human GRCh38 chr10: 8,067,341-8,067,355 , GRCh37.p13 chr10: 8,109,304-8,109,318 GATA3
    nsv4969515copy number variation1nstd200human GRCh38 chr10: 8,068,271-8,069,386 , GRCh37.p13 chr10: 8,110,234-8,111,349 GATA3
    nsv4832382copy number variation1nstd200human GRCh37 chr10: 8,110,234-8,111,349 , GRCh38.p12 chr10: 8,068,271-8,069,386 GATA3
    nsv4668805copy number variation1nstd186human GRCh37 chr10: 8,089,501-8,097,500 , GRCh38.p12 chr10: 8,047,538-8,055,537 , GATA3, 1 more genes
    nsv4615604copy number variation1nstd183human GRCh37 chr10: 7,507,804-8,203,475 , GRCh38.p12 chr10: 7,465,842-8,161,512 , LINC02642, 14 more genes
    nsv4602220copy number variation1nstd183human GRCh37 chr10: 8,089,501-8,097,500 , GRCh38.p12 chr10: 8,047,538-8,055,537 , GATA3-AS1, 1 more genes
    nsv4479413mobile element insertion1nstd166human GRCh37.p13 chr10: 8,108,324-8,108,324 , GRCh38.p12 chr10: 8,066,361-8,066,361 GATA3
    nsv4456896copy number variation1nstd102humanUncertain significance GRCh37 chr10: 8,075,029-8,407,665 , GRCh38.p12 chr10: 8,033,066-8,365,702 LOC107984205, LOC105376394, 6 more genes
    nsv4455884copy number variation1nstd102humanPathogenic GRCh37 chr10: 8,011,156-9,996,086 , GRCh38.p12 chr10: 7,969,193-9,954,123 LOC105376396, KRT8P37, 22 more genes
    nsv4455607copy number variation2nstd102humanPathogenic GRCh37 chr10: 100,026-15,273,144 , GRCh38.p12 chr10: 54,086-15,231,145 LOC105376357, LINC02649, 264 more genes
    nsv3924406copy number variation1nstd102humanPathogenic GRCh38 chr10: 69,261-19,184,047 , GRCh37 chr10: 224,406-19,472,976 , NCBI36 chr10: 105,201-19,512,982 WDR37, LOC105376364, 302 more genes
    nsv3923991copy number variation1nstd102humanLikely pathogenic NCBI36 chr10: 1,633,367-9,285,698 , GRCh37 chr10: 1,643,367-9,245,692 , GRCh38 chr10: 1,601,172-9,203,729 ADARB2, ATP5F1C, 143 more genes
    nsv3923974copy number variation1nstd102humanPathogenic NCBI36 chr10: 109,796-12,897,920 , GRCh38 chr10: 73,856-12,815,915 , GRCh37 chr10: 119,796-12,857,914 LINC02663, LARP4B-DT, 208 more genes
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