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Items: 1 to 20 of 149

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5970408inversion1nstd209human GRCh38 chr19: 2,282,477-7,636,587 , GRCh37.p13 chr19: 2,282,476-7,701,473 , TLE5, 195 more genes
    nsv5942775copy number variation1nstd209human GRCh38 chr19: 2,865,023-7,153,898 , GRCh37.p13 chr19: 2,865,021-7,153,909 , GNA15-DT, 159 more genes
    nsv5935711copy number variation1nstd209human GRCh38 chr19: 4,642,371-4,643,271 , GRCh37.p13 chr19: 4,642,383-4,643,283 TNFAIP8L1
    nsv5927986copy number variation1nstd209human GRCh38 chr19: 4,651,416-4,651,539 , GRCh37.p13 chr19: 4,651,428-4,651,551 TNFAIP8L1
    nsv5885291copy number variation1nstd209human GRCh38 chr19: 4,653,793-4,655,092 , GRCh37.p13 chr19: 4,653,805-4,655,104 TNFAIP8L1
    nsv5517859copy number variation1nstd206human GRCh38 chr19: 4,651,438-4,651,540 , GRCh37.p13 chr19: 4,651,450-4,651,552 TNFAIP8L1
    nsv5292408copy number variation1nstd204human GRCh38.p13 chr19: 2,552,101-4,875,100 , GRCh37.p13 chr19: 2,552,099-4,875,112 , S1PR4, 93 more genes
    nsv5027354copy number variation1nstd200human GRCh38 chr19: 4,653,070-4,656,954 , GRCh37.p13 chr19: 4,653,082-4,656,966 TNFAIP8L1, MYDGF
    nsv5027353copy number variation1nstd200human GRCh38 chr19: 4,642,371-4,643,272 , GRCh37.p13 chr19: 4,642,383-4,643,284 TNFAIP8L1
    nsv5027352copy number variation1nstd200human GRCh38 chr19: 4,641,610-4,642,385 , GRCh37.p13 chr19: 4,641,622-4,642,397 TNFAIP8L1
    nsv5027346copy number variation1nstd200human GRCh38 chr19: 4,601,780-4,649,655 , GRCh37.p13 chr19: 4,601,792-4,649,667 LOC100287614, TNFAIP8L1
    nsv4852684copy number variation1nstd200human GRCh37 chr19: 4,642,383-4,643,284 , GRCh38.p12 chr19: 4,642,371-4,643,272 TNFAIP8L1
    nsv4852683copy number variation1nstd200human GRCh37 chr19: 4,641,622-4,642,397 , GRCh38.p12 chr19: 4,641,610-4,642,385 TNFAIP8L1
    nsv4457776copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,911-4,788,357 , GRCh38.p12 chr19: 260,911-4,788,345 BSG, LOC100420586, 217 more genes
    nsv4350537copy number variation1nstd102humanPathogenic GRCh37 chr19: 3,076,808-4,796,782 , GRCh38.p12 chr19: 3,076,810-4,796,770 FEM1A, MIR7-3, 70 more genes
    nsv4271833copy number variation1nstd166human GRCh37.p13 chr19: 4,641,622-4,642,397 , GRCh38.p12 chr19: 4,641,610-4,642,385 TNFAIP8L1
    nsv4264483copy number variation1nstd166human GRCh37.p13 chr19: 4,645,933-4,645,989 , GRCh38.p12 chr19: 4,645,921-4,645,977 TNFAIP8L1
    nsv4252465copy number variation1nstd166human GRCh37.p13 chr19: 4,651,450-4,651,552 , GRCh38.p12 chr19: 4,651,438-4,651,540 TNFAIP8L1
    nsv3924102copy number variation1nstd102humanPathogenic GRCh38 chr19: 259,395-6,795,611 , GRCh37 chr19: 259,395-6,795,622 , NCBI36 chr19: 210,395-6,746,622 POLR2E, PWWP3A, 283 more genes
    nsv3923885copy number variation1nstd102humanPathogenic GRCh38 chr19: 4,008,560-4,763,159 , GRCh37 chr19: 4,008,558-4,763,171 , NCBI36 chr19: 3,959,558-4,714,171 MIR4746, HDGFL2, 30 more genes
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