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Items: 1 to 20 of 87

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7143098copy number variation1nstd232human GRCh38.p12 chr19: 10,115,584-10,115,681 , GRCh37.p13 chr19: 10,226,260-10,226,357 P2RY11, EIF3G, 1 more genes
    nsv7141467copy number variation1nstd232human GRCh38.p12 chr19: 10,110,611-10,110,692 , GRCh37.p13 chr19: 10,221,287-10,221,368 P2RY11, PPAN, 1 more genes
    nsv7141123copy number variation1nstd232human GRCh38.p12 chr19: 10,110,865-10,110,942 , GRCh37.p13 chr19: 10,221,541-10,221,618 P2RY11, PPAN, 1 more genes
    nsv7062606inversion1nstd229human GRCh38 chr19: 10,024,335-10,946,724 , GRCh37.p13 chr19: 10,135,011-11,057,400 FDX2, ICAM4, 48 more genes
    nsv6999748copy number variation1nstd229human GRCh38 chr19: 10,102,367-10,133,810 , GRCh37.p13 chr19: 10,213,043-10,244,486 EIF3G, SNORD105, 6 more genes
    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
    nsv6528510copy number variation1nstd223human GRCh38 chr19: 10,102,367-10,133,807 , GRCh37.p13 chr19: 10,213,043-10,244,483 PPAN, ANGPTL6, 6 more genes
    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
    nsv5529449copy number variation1nstd206human GRCh38 chr19: 10,111,992-10,112,181 , GRCh37.p13 chr19: 10,222,668-10,222,857 PPAN-P2RY11, P2RY11, 1 more genes
    nsv5284255copy number variation1nstd204human GRCh38.p13 chr19: 10,061,101-10,331,300 , GRCh37.p13 chr19: 10,171,777-10,441,976 ICAM1, ICAM4, 19 more genes
    nsv5014498copy number variation1nstd200human GRCh38 chr19: 10,102,367-10,133,810 , GRCh37.p13 chr19: 10,213,043-10,244,486 SNORD105B, P2RY11, 6 more genes
    nsv5011585copy number variation1nstd200human GRCh38 chr19: 10,114,498-10,114,599 , GRCh37.p13 chr19: 10,225,174-10,225,275 EIF3G, P2RY11, 1 more genes
    nsv4864914copy number variation1nstd200human GRCh37 chr19: 10,213,043-10,244,486 , GRCh38.p12 chr19: 10,102,367-10,133,810 ANGPTL6, P2RY11, 6 more genes
    nsv4679505copy number variation1nstd189human GRCh37.p13 chr19: 9,903,732-10,322,986 , GRCh38.p12 chr19: 9,793,056-10,212,310 DNMT1, P2RY11, 18 more genes
    nsv4624262copy number variation1nstd183human GRCh37 chr19: 10,218,959-10,370,939 , GRCh38.p12 chr19: 10,108,283-10,260,263 EIF3G, MIR4322, 9 more genes
    nsv4375402copy number variation1nstd173human GRCh37 chr19: 9,970,367-10,250,655 , GRCh38.p12 chr19: 9,859,691-10,139,979 P2RY11, RDH8, 12 more genes
    nsv4264683copy number variation1nstd166human GRCh37.p13 chr19: 10,219,886-10,239,223 , GRCh38.p12 chr19: 10,109,210-10,128,547 PPAN-P2RY11, PPAN, 3 more genes
    nsv4258124copy number variation1nstd166human GRCh37.p13 chr19: 10,211,551-10,232,005 , GRCh38.p12 chr19: 10,100,875-10,121,329 P2RY11, EIF3G, 5 more genes
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