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Items: 1 to 20 of 134

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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
    nsv5553158insertion1nstd206human GRCh38 chr19: 4,448,970-4,448,970 , GRCh37.p13 chr19: 4,448,967-4,448,967 UBXN6
    nsv5518701copy number variation1nstd206human GRCh38 chr19: 4,458,630-4,459,878 , GRCh37.p13 chr19: 4,458,627-4,459,875 UBXN6
    nsv5320848copy number variation1nstd204human GRCh38.p13 chr19: 4,440,840-4,449,997 , GRCh37.p13 chr19: 4,440,837-4,449,994 MIR4746, CHAF1A, 1 more genes
    nsv5292942copy number variation1nstd204human GRCh38.p13 chr19: 4,440,888-4,449,939 , GRCh37.p13 chr19: 4,440,885-4,449,936 UBXN6, MIR4746, 1 more genes
    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
    nsv5284500copy number variation1nstd204human GRCh38.p13 chr19: 4,068,001-4,541,200 , GRCh37.p13 chr19: 4,067,999-4,541,212 , EIF1P6, 20 more genes
    nsv5163496mobile element insertion1nstd203human GRCh38 chr19: 4,459,229-4,459,278 , GRCh37.p13 chr19: 4,459,226-4,459,275 UBXN6
    nsv5027328copy number variation1nstd200human GRCh38 chr19: 4,458,619-4,460,317 , GRCh37.p13 chr19: 4,458,616-4,460,314 UBXN6
    nsv4864846copy number variation1nstd200human GRCh37 chr19: 4,440,843-4,449,991 , GRCh38.p12 chr19: 4,440,846-4,449,994 MIR4746, CHAF1A, 1 more genes
    nsv4537627copy number variation1nstd166human GRCh37.p13 chr19: 4,459,244-4,459,779 , GRCh38.p12 chr19: 4,459,247-4,459,782 UBXN6
    nsv4457776copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,911-4,788,357 , GRCh38.p12 chr19: 260,911-4,788,345 BSG, LOC100420586, 217 more genes
    nsv4373071copy number variation1nstd173human GRCh37 chr19: 4,370,912-4,514,073 , GRCh38.p12 chr19: 4,370,915-4,514,061 , SH3GL1, 5 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
    nsv4267479copy number variation1nstd166human GRCh37.p13 chr19: 4,339,885-4,577,030 , GRCh38.p12 chr19: 4,339,888-4,577,018 , UBXN6, 11 more genes
    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
    nsv3923561copy number variation1nstd102humanPathogenic NCBI36 chr19: 184,565-4,650,484 , GRCh37 chr19: 233,565-4,699,484 , GRCh38 chr19: 233,565-4,699,472 DAPK3, IZUMO4, 214 more genes
    nsv3921377copy number variation1nstd102humanUncertain significance NCBI36 chr19: 4,368,983-4,672,878 , GRCh38 chr19: 4,417,986-4,721,866 , GRCh37 chr19: 4,417,983-4,721,878 MIR4746, SEMA6B, 13 more genes
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