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Items: 1 to 20 of 193

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5943312copy number variation1nstd209human GRCh38 chr19: 47,359,638-47,359,899 , GRCh37.p13 chr19: 47,862,895-47,863,156 DHX34
    nsv5521456copy number variation1nstd206human GRCh38 chr19: 47,351,968-47,352,063 , GRCh37.p13 chr19: 47,855,225-47,855,320 DHX34
    nsv5521439copy number variation1nstd206human GRCh38 chr19: 47,349,396-47,349,446 , GRCh37.p13 chr19: 47,852,653-47,852,703 DHX34
    nsv5521029copy number variation1nstd206human GRCh38 chr19: 47,346,534-47,348,091 , GRCh37.p13 chr19: 47,849,791-47,851,348 C5AR2, DHX34
    nsv5520367copy number variation1nstd206human GRCh38 chr19: 47,368,608-47,368,670 , GRCh37.p13 chr19: 47,871,865-47,871,927 DHX34
    nsv5380260translocation1nstd200human GRCh38 chr19: 47,347,504-47,347,504 , GRCh38 chr19: 3,123,366-3,123,366 , GRCh37.p13 chr19: 3,123,364-3,123,364 , GRCh37.p13 chr19: 47,850,761-47,850,761 GNA11, DHX34, 1 more genes
    nsv5359867translocation1nstd200human GRCh38 chr19: 47,355,036-47,355,036 , GRCh38 chr19: 47,736,006-47,736,006 , GRCh37.p13 chr19: 47,858,293-47,858,293 , GRCh37.p13 chr19: 48,239,263-48,239,263 EHD2, DHX34
    nsv5293275copy number variation1nstd204human GRCh38.p13 chr19: 47,049,201-47,476,100 , GRCh37.p13 chr19: 47,552,459-47,979,357 , ZC3H4, 12 more genes
    nsv5287634copy number variation1nstd204human GRCh38.p13 chr19: 47,201,401-47,396,100 , GRCh37.p13 chr19: 47,704,658-47,899,357 , DHX34, 8 more genes
    nsv5024764copy number variation1nstd200human GRCh38 chr19: 47,328,635-47,354,871 , GRCh37.p13 chr19: 47,831,892-47,858,128 DHX34, C5AR2
    nsv5020837copy number variation1nstd200human GRCh38 chr19: 47,364,860-47,378,357 , GRCh37.p13 chr19: 47,868,117-47,881,614 DHX34
    nsv5020836copy number variation1nstd200human GRCh38 chr19: 47,350,697-47,353,385 , GRCh37.p13 chr19: 47,853,954-47,856,642 DHX34
    nsv5020835copy number variation1nstd200human GRCh38 chr19: 47,347,445-47,348,345 , GRCh37.p13 chr19: 47,850,702-47,851,602 DHX34, C5AR2
    nsv4865227copy number variation1nstd200human GRCh37 chr19: 47,831,892-47,858,128 , GRCh38.p12 chr19: 47,328,635-47,354,871 C5AR2, DHX34
    nsv4853192copy number variation1nstd200human GRCh37 chr19: 47,868,117-47,881,614 , GRCh38.p12 chr19: 47,364,860-47,378,357 DHX34
    nsv4853191copy number variation1nstd200human GRCh37 chr19: 47,850,702-47,851,602 , GRCh38.p12 chr19: 47,347,445-47,348,345 C5AR2, DHX34
    nsv4676357copy number variation1nstd102humanPathogenic GRCh37 chr19: 44,738,088-53,621,561 , GRCh38.p12 chr19: 44,233,935-53,118,308 MIR4324, KLK9, 485 more genes
    nsv4676350copy number variation1nstd102humanUncertain significance GRCh37 chr19: 45,531,056-48,174,177 , GRCh38.p12 chr19: 45,027,798-47,670,920 NKPD1, IGFL1, 112 more genes
    nsv4676254copy number variation1nstd102humanUncertain significance GRCh37 chr19: 47,331,662-48,234,260 , GRCh38.p12 chr19: 46,828,405-47,731,003 AP2S1, BICRA, 22 more genes
    nsv4629839copy number variation1nstd183human GRCh37 chr19: 47,836,615-47,885,282 , GRCh38.p12 chr19: 47,333,358-47,382,025 DHX34, C5AR2
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