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Items: 1 to 20 of 177

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7062606inversion1nstd229human GRCh38 chr19: 10,024,335-10,946,724 , GRCh37.p13 chr19: 10,135,011-11,057,400 FDX2, ICAM4, 48 more genes
    nsv7017512copy number variation1nstd229human GRCh38 chr19: 10,054,855-10,069,784 , GRCh37.p13 chr19: 10,165,531-10,180,460 C3P1
    nsv7011591copy number variation1nstd229human GRCh38 chr19: 9,998,374-10,104,214 , GRCh37.p13 chr19: 10,109,050-10,214,890 MIR5589, RDH8, 4 more genes
    nsv7008931copy number variation1nstd229human GRCh38 chr19: 10,050,601-10,057,300 , GRCh37.p13 chr19: 10,161,277-10,167,976 C3P1
    nsv7008589copy number variation1nstd229human GRCh38 chr19: 10,013,601-10,069,100 , GRCh37.p13 chr19: 10,124,277-10,179,776 MIR5589, C3P1, 1 more genes
    nsv7008277copy number variation1nstd229human GRCh38 chr19: 10,069,583-10,072,036 , GRCh37.p13 chr19: 10,180,259-10,182,712 C3P1
    nsv7007832copy number variation1nstd229human GRCh38 chr19: 10,051,624-10,066,125 , GRCh37.p13 chr19: 10,162,300-10,176,801 C3P1
    nsv7005449copy number variation1nstd229human GRCh38 chr19: 10,008,846-10,039,555 , GRCh37.p13 chr19: 10,119,522-10,150,231 C3P1, MIR5589, 2 more genes
    nsv7002120copy number variation1nstd229human GRCh38 chr19: 10,007,238-10,042,099 , GRCh37.p13 chr19: 10,117,914-10,152,775 C3P1, MIR5589, 2 more genes
    nsv6998814copy number variation1nstd229human GRCh38 chr19: 10,033,035-10,047,405 , GRCh37.p13 chr19: 10,143,711-10,158,081 MIR5589, C3P1
    nsv6998259copy number variation1nstd229human GRCh38 chr19: 10,046,601-11,033,768 , GRCh37.p13 chr19: 10,157,277-11,144,444 MRPL4, QTRT1, 49 more genes
    nsv6599932inversion1nstd223human GRCh38 chr19: 10,059,350-10,060,088 , GRCh37.p13 chr19: 10,170,026-10,170,764 C3P1
    nsv6534613copy number variation1nstd223human GRCh38 chr19: 10,066,696-10,075,103 , GRCh37.p13 chr19: 10,177,372-10,185,779 C3P1
    nsv6531448copy number variation1nstd223human GRCh38 chr19: 10,069,583-10,072,037 , GRCh37.p13 chr19: 10,180,259-10,182,713 C3P1
    nsv6521264copy number variation1nstd223human GRCh38 chr19: 10,053,501-10,057,700 , GRCh37.p13 chr19: 10,164,177-10,168,376 C3P1
    nsv6517055copy number variation1nstd223human GRCh38 chr19: 10,064,460-10,065,462 , GRCh37.p13 chr19: 10,175,136-10,176,138 C3P1
    nsv6516820copy number variation1nstd223human GRCh38 chr19: 10,049,801-10,056,700 , GRCh37.p13 chr19: 10,160,477-10,167,376 C3P1
    nsv6291543copy number variation1nstd102humanUncertain significance GRCh37 chr19: 9,941,033-11,739,567 , GRCh38.p12 chr19: 9,830,357-11,628,752 KRI1, SHFL, 88 more genes
    nsv6133698copy number variation1nstd213human GRCh37 chr19: 2,900,000-11,490,001 , GRCh38.p12 chr19: 2,900,002-11,379,325 , TLE5, 341 more genes
    nsv6133479copy number variation1nstd213human GRCh37 chr19: 7,400,000-13,280,001 , GRCh38.p12 chr19: 7,335,095-13,169,187 , ACP5, 299 more genes
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