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Items: 1 to 20 of 71

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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
    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
    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
    nsv5282992copy number variation1nstd204human GRCh38.p13 chr19: 10,101,101-10,105,700 , GRCh37.p13 chr19: 10,211,777-10,216,376 PPAN, ANGPTL6, 2 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
    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
    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
    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
    nsv3920616copy number variation1nstd102humanLikely pathogenic NCBI36 chr19: 8,802,823-13,303,041 , GRCh37 chr19: 8,941,823-13,442,041 , GRCh38 chr19: 8,831,147-13,331,227 ACP5, GET3, 236 more genes
    nsv3912242copy number variation1nstd102humanPathogenic GRCh37 chr19: 9,846,119-11,338,677 , GRCh38 chr19: 9,735,443-11,228,001 , NCBI36 chr19: 9,707,119-11,199,677 PPAN, S1PR5, 68 more genes
    nsv3904885copy number variation1nstd102humanPathogenic GRCh37 chr19: 68,029-59,110,290 , GRCh38.p12 chr19: 68,029-58,598,923 ZNF321P, ZNF861P, 2443 more genes
    nsv3903203copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,912-59,097,160 , GRCh38.p12 chr19: 260,912-58,585,793 BABAM1, BEST2, 2426 more genes
    nsv3903092copy number variation2nstd102humanPathogenic GRCh37 chr19: 260,912-58,956,888 , GRCh38.p12 chr19: 260,912-58,445,521 LENG8, SYDE1, 2408 more genes
    nsv3898900copy number variation1nstd102humanPathogenic GRCh37 chr19: 9,678,768-14,853,426 , GRCh38.p12 chr19: 9,568,092-14,742,614 FBXL12, DCAF15, 253 more genes
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