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Items: 1 to 20 of 274

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5521400copy number variation1nstd206human GRCh38 chr19: 737,471-844,853 , GRCh37.p13 chr19: 737,471-844,853 PTBP1, PALM, 8 more genes
    nsv5359357translocation1nstd200human GRCh38 chr19: 803,082-803,082 , GRCh38 chr19: 802,977-802,977 , GRCh37.p13 chr19: 802,977-802,977 , GRCh37.p13 chr19: 803,082-803,082 PTBP1, MIR4745
    nsv5327588copy number variation1nstd204human GRCh38.p13 chr19: 502,284-1,164,314 , GRCh37.p13 chr19: 502,284-1,164,313 RPS2P52, PRSS57, 44 more genes
    nsv5285258copy number variation1nstd204human GRCh38.p13 chr19: 667,301-878,200 , GRCh37.p13 chr19: 667,301-878,200 FSTL3, ELANE, 14 more genes
    nsv5029164copy number variation1nstd200human GRCh38 chr19: 502,290-1,164,305 , GRCh37.p13 chr19: 502,290-1,164,304 LOC105372235, RNU6-2, 44 more genes
    nsv4854867copy number variation1nstd200human GRCh37 chr19: 502,290-1,164,304 , GRCh38.p12 chr19: 502,290-1,164,305 LOC100420586, BSG, 44 more genes
    nsv4683365copy number variation1nstd102humanUncertain significance GRCh37 chr19: 589,926-1,401,495 , GRCh38.p12 chr19: 589,926-1,401,496 MISP, STK11, 56 more genes
    nsv4676346copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,911-3,501,271 , GRCh38.p12 chr19: 260,911-3,501,273 AZU1, REEP6, 159 more genes
    nsv4676189copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,912-4,384,674 , GRCh38.p12 chr19: 260,912-4,384,677 MRPL54, DAZAP1, 198 more genes
    nsv4457776copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,911-4,788,357 , GRCh38.p12 chr19: 260,911-4,788,345 BSG, LOC100420586, 217 more genes
    nsv4420020copy number variation1nstd174human GRCh37 chr19: 794,878-815,173 , GRCh38.p12 chr19: 794,878-815,173 PTBP1, PLPPR3, 2 more genes
    nsv4270630copy number variation1nstd166human GRCh37.p13 chr19: 723,480-804,663 , GRCh38.p12 chr19: 723,480-804,663 PALM, PTBP1, 4 more genes
    nsv4265380copy number variation1nstd166human GRCh37.p13 chr19: 784,000-805,000 , GRCh38.p12 chr19: 784,000-805,000 MIR4745, LINC01836, 1 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
    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
    nsv3923328copy number variation1nstd102humanPathogenic GRCh37 chr19: 259,395-819,679 , NCBI36 chr19: 210,395-770,679 , GRCh38 chr19: 259,395-819,679 LOC100420586, CDC34, 31 more genes
    nsv3922550copy number variation1nstd102humanPathogenic GRCh38 chr19: 259,395-1,952,650 , GRCh37 chr19: 259,395-1,952,649 , NCBI36 chr19: 210,395-1,903,649 LOC102723811, DAZAP1, 99 more genes
    nsv3922156copy number variation1nstd102humanPathogenic GRCh38 chr19: 591,812-1,358,152 , GRCh37 chr19: 591,812-1,358,151 , NCBI36 chr19: 542,812-1,309,151 ARID3A, EFNA2, 52 more genes
    nsv3921941copy number variation1nstd102humanUncertain significance GRCh38 chr19: 677,680-899,104 , GRCh37 chr19: 677,680-899,104 , NCBI36 chr19: 628,680-850,104 LOC101928450, AZU1, 16 more genes
    nsv3921932copy number variation1nstd102humanPathogenic NCBI36 chr19: 210,395-2,506,147 , GRCh37 chr19: 259,395-2,555,147 , GRCh38 chr19: 259,395-2,555,149 GZMM, MIER2, 129 more genes
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