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Items: 1 to 20 of 952

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148130copy number variation1nstd102humanPathogenic GRCh37 chr8: 36,763,176-50,929,707 , GRCh38.p12 chr8: 36,905,658-50,017,147 SNTG1, RN7SL806P, 193 more genes
    nsv7075375inversion1nstd229human GRCh38 chr8: 39,470,316-39,486,210 , GRCh37.p13 chr8: 39,327,835-39,343,729 ADAM3A
    nsv7069051inversion1nstd229human GRCh38 chr8: 39,481,006-39,481,074 , GRCh37.p13 chr8: 39,338,525-39,338,593 ADAM3A
    nsv7061029inversion1nstd229human GRCh38 chr8: 39,470,722-39,482,739 , GRCh37.p13 chr8: 39,328,241-39,340,258 ADAM3A
    nsv6857533copy number variation1nstd229human GRCh38 chr8: 39,401,101-39,529,700 , GRCh37.p13 chr8: 39,258,620-39,387,219 ADAM5, ADAM3A
    nsv6856965copy number variation1nstd229human GRCh38 chr8: 39,374,556-39,529,710 , GRCh37.p13 chr8: 39,232,075-39,387,229 ADAM5, ADAM3A
    nsv6849377copy number variation1nstd229human GRCh38 chr8: 39,379,601-39,529,700 , GRCh37.p13 chr8: 39,237,120-39,387,219 ADAM5, ADAM3A
    nsv6845661copy number variation1nstd229human GRCh38 chr8: 39,374,501-39,505,500 , GRCh37.p13 chr8: 39,232,020-39,363,019 ADAM5, ADAM3A
    nsv6843289copy number variation1nstd229human GRCh38 chr8: 39,514,498-39,514,541 , GRCh37.p13 chr8: 39,372,017-39,372,060 ADAM3A
    nsv6843047copy number variation1nstd229human GRCh38 chr8: 39,462,473-39,462,525 , GRCh37.p13 chr8: 39,319,992-39,320,044 ADAM3A
    nsv6843026copy number variation1nstd229human GRCh38 chr8: 39,522,448-39,522,477 , GRCh37.p13 chr8: 39,379,967-39,379,996 ADAM3A
    nsv6839650copy number variation1nstd229human GRCh38 chr8: 38,572,201-41,442,522 , GRCh37.p13 chr8: 38,429,719-41,300,041 RPL3P10, SNORD65B, 35 more genes
    nsv6634301complex substitution1nstd102humanPathogenic GRCh38.p12 chr8: 208,048-43,132,174 , GRCh37 chr8: 158,048-42,987,317 NAT1, NAT2, 758 more genes
    nsv6632982copy number variation1nstd224human GRCh37 chr8: 38,762,056-39,892,501 , GRCh38.p12 chr8: 38,904,538-40,034,982 , GRCh38.p12 chr8|NT_187577.1: 1-624,492 ADAM9, SNORD38D, 15 more genes
    nsv6426776copy number variation1nstd223human GRCh38 chr8: 39,373,201-39,529,700 , GRCh37.p13 chr8: 39,230,720-39,387,219 ADAM5, ADAM3A
    nsv6426563copy number variation1nstd223human GRCh38 chr8: 39,496,571-39,498,962 , GRCh37.p13 chr8: 39,354,090-39,356,481 ADAM3A
    nsv6426142copy number variation1nstd223human GRCh38 chr8: 39,362,001-39,529,700 , GRCh37.p13 chr8: 39,219,520-39,387,219 ADAM5, ADAM3A
    nsv6421068copy number variation1nstd223human GRCh38 chr8: 39,453,319-39,453,554 , GRCh37.p13 chr8: 39,310,838-39,311,073 ADAM3A
    nsv6419510copy number variation1nstd223human GRCh38 chr8: 39,359,801-39,578,400 , GRCh37.p13 chr8: 39,217,320-39,435,919 ADAM3A, LOC100130964, 1 more genes
    nsv6418680copy number variation1nstd223human GRCh38 chr8: 39,492,501-39,638,000 , GRCh37.p13 chr8: 39,350,020-39,495,519 ADAM18, ADAM3A, 1 more genes
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