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Items: 1 to 20 of 87

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5555882sequence alteration1nstd206human GRCh38 chr19: 45,580,124-46,272,839 , GRCh37.p13 chr19: 46,083,382-46,776,096 , SYMPK, 39 more genes
    nsv5518171copy number variation1nstd206human GRCh38 chr19: 45,941,663-45,943,480 , GRCh37.p13 chr19: 46,444,921-46,446,738 NOVA2
    nsv5375466translocation1nstd200human GRCh38 chr19: 45,943,443-45,943,443 , GRCh38 chr19: 45,941,715-45,941,715 , GRCh37.p13 chr19: 46,444,973-46,444,973 , GRCh37.p13 chr19: 46,446,701-46,446,701 NOVA2
    nsv5297939copy number variation1nstd204human GRCh38.p13 chr19: 45,948,948-45,951,682 , GRCh37.p13 chr19: 46,452,206-46,454,940 NOVA2
    nsv5024734copy number variation1nstd200human GRCh38 chr19: 45,967,911-45,971,226 , GRCh37.p13 chr19: 46,471,169-46,474,484 NOVA2
    nsv5020730copy number variation1nstd200human GRCh38 chr19: 45,964,518-45,965,246 , GRCh37.p13 chr19: 46,467,776-46,468,504 NOVA2
    nsv5020729copy number variation1nstd200human GRCh38 chr19: 45,946,821-45,948,439 , GRCh37.p13 chr19: 46,450,079-46,451,697 NOVA2
    nsv4853107copy number variation1nstd200human GRCh37 chr19: 46,460,575-46,461,106 , GRCh38.p12 chr19: 45,957,317-45,957,848 NOVA2
    nsv4853106copy number variation1nstd200human GRCh37 chr19: 46,444,881-46,446,779 , GRCh38.p12 chr19: 45,941,623-45,943,521 NOVA2
    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
    nsv4667807copy number variation1nstd186human GRCh37 chr19: 46,444,942-46,446,779 , GRCh38.p12 chr19: 45,941,684-45,943,521 NOVA2
    nsv4626638copy number variation1nstd183human GRCh37 chr19: 46,444,942-46,446,779 , GRCh38.p12 chr19: 45,941,684-45,943,521 NOVA2
    nsv4457372copy number variation1nstd102humanPathogenic GRCh37 chr19: 28,271,106-49,213,832 , GRCh38.p12 chr19: 27,780,198-48,710,575 ZNF461, LOC101927572, 735 more genes
    nsv3924836copy number variation1nstd102humanPathogenic NCBI36 chr19: 50,166,517-53,452,471 , GRCh37 chr19: 45,474,677-48,760,659 , GRCh38 chr19: 44,971,420-48,257,402 IGFL1P1, LOC105372426, 145 more genes
    nsv3921787copy number variation1nstd102humanLikely pathogenic NCBI36 chr19: 50,582,487-52,026,097 , GRCh37 chr19: 45,890,647-47,334,257 , GRCh38 chr19: 45,387,389-46,831,000 CALM3, DMPK, 71 more genes
    nsv3916206copy number variation1nstd102humanPathogenic GRCh37 chr19: 46,099,131-47,103,283 , NCBI36 chr19: 50,790,971-51,795,123 , GRCh38 chr19: 45,595,873-46,600,026 PNMA8B, MIR642B, 47 more genes
    nsv3905567copy number variation1nstd102humanUncertain significance GRCh37 chr19: 46,361,535-46,573,564 , GRCh38.p12 chr19: 45,858,277-46,070,306 NANOS2, CCDC61, 9 more genes
    nsv3904885copy number variation1nstd102humanPathogenic GRCh37 chr19: 68,029-59,110,290 , GRCh38.p12 chr19: 68,029-58,598,923 ZNF321P, ZNF861P, 2443 more genes
    nsv3903203copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,912-59,097,160 , GRCh38.p12 chr19: 260,912-58,585,793 BABAM1, BEST2, 2426 more genes
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