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Items: 1 to 20 of 22

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6291587copy number variation1nstd102humanPathogenic GRCh37 chr19: 3,501,624-5,357,124 , GRCh38.p12 chr19: 3,501,626-5,357,113 STAP2, RN7SL202P, 67 more genes
    nsv4350537copy number variation1nstd102humanPathogenic GRCh37 chr19: 3,076,808-4,796,782 , GRCh38.p12 chr19: 3,076,810-4,796,770 STAP2, FEM1A, 70 more genes
    nsv3915152copy number variation1nstd102humanPathogenic NCBI36 chr19: 3,289,022-4,784,151 , GRCh38 chr19: 3,338,024-4,833,139 , GRCh37 chr19: 3,338,022-4,833,151 STAP2, APBA3, 63 more genes
    nsv3910627copy number variation1nstd102humanPathogenic GRCh37 chr19: 3,554,633-4,690,977 , NCBI36 chr19: 3,505,633-4,641,977 , GRCh38 chr19: 3,554,635-4,690,965 STAP2, PIAS4, 49 more genes
    nsv5381793copy number variation1nstd102humanPathogenic GRCh37 chr19: 3,976,203-4,345,430 , GRCh38.p12 chr19: 3,976,205-4,345,433 STAP2, MPND, 13 more genes
    nsv3904885copy number variation1nstd102humanPathogenic GRCh37 chr19: 68,029-59,110,290 , GRCh38.p12 chr19: 68,029-58,598,923 STAP2, ZNF321P, 2443 more genes
    nsv3903203copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,912-59,097,160 , GRCh38.p12 chr19: 260,912-58,585,793 STAP2, BABAM1, 2426 more genes
    nsv3903092copy number variation2nstd102humanPathogenic GRCh37 chr19: 260,912-58,956,888 , GRCh38.p12 chr19: 260,912-58,445,521 STAP2, LENG8, 2408 more genes
    nsv3914351copy number variation1nstd102humanPathogenic NCBI36 chr19: 1,923,244-9,620,555 , GRCh38 chr19: 1,972,245-9,648,879 , GRCh37 chr19: 1,972,244-9,759,555 STAP2, SEMA6B, 299 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 STAP2, POLR2E, 283 more genes
    nsv3890584copy number variation1nstd102humanPathogenic GRCh37 chr19: 3,120,160-9,732,820 , GRCh38.p12 chr19: 3,120,162-9,622,144 STAP2, PCP2, 250 more genes
    nsv4457776copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,911-4,788,357 , GRCh38.p12 chr19: 260,911-4,788,345 STAP2, BSG, 217 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 STAP2, DAPK3, 214 more genes
    nsv4676189copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,912-4,384,674 , GRCh38.p12 chr19: 260,912-4,384,677 STAP2, MRPL54, 198 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 STAP2, MIR4746, 30 more genes
    nsv3918318copy number variation1nstd102humanLikely pathogenic NCBI36 chr19: 3,739,725-5,098,365 , GRCh37 chr19: 3,788,725-5,147,365 , GRCh38 chr19: 3,788,727-5,147,354 STAP2, DAPK3, 49 more genes
    nsv3910993copy number variation1nstd102humanLikely pathogenic NCBI36 chr19: 3,031,619-4,863,634 , GRCh37 chr19: 3,080,619-4,912,634 , GRCh38 chr19: 3,080,621-4,912,622 STAP2, DAPK3, 74 more genes
    nsv7095297copy number variation1nstd102humanUncertain significance GRCh37 chr19: 589,946-5,696,788 , GRCh38.p12 chr19: 589,946-5,696,777 STAP2, NCLN, 223 more genes
    nsv7095226copy number variation1nstd102humanUncertain significance GRCh37 chr19: 589,946-4,818,389 , GRCh38.p12 chr19: 589,946-4,818,377 STAP2, ATP5F1D, 204 more genes
    nsv3921092copy number variation1nstd102humanUncertain significance GRCh38 chr19: 3,947,934-5,196,676 , GRCh37 chr19: 3,947,932-5,196,687 , NCBI36 chr19: 3,898,932-5,147,687 STAP2, FEM1A, 43 more genes
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