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Items: 1 to 20 of 94

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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
    nsv5327341copy number variation1nstd204human GRCh38.p13 chr19: 45,584,936-45,884,300 , GRCh37.p13 chr19: 46,088,194-46,387,558 DMWD, GPR4, 19 more genes
    nsv5299705copy number variation1nstd204human GRCh38.p13 chr19: 45,762,896-45,768,445 , GRCh37.p13 chr19: 46,266,154-46,271,703 MEIOSIN, SIX5, 2 more genes
    nsv5284788copy number variation1nstd204human GRCh38.p13 chr19: 45,504,601-45,776,400 , GRCh37.p13 chr19: 46,007,859-46,279,658 MIR642A, LOC107985315, 17 more genes
    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
    nsv4630966copy number variation1nstd183human GRCh37 chr19: 46,262,948-46,268,113 , GRCh38.p12 chr19: 45,759,690-45,764,855 SIX5, MEIOSIN
    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
    nsv3957331insertion1nstd168human GRCh38 chr19: 45,731,226-45,783,390 , GRCh37.p13 chr19: 46,234,484-46,286,648 DMPK, DMWD, 4 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
    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
    nsv3903092copy number variation2nstd102humanPathogenic GRCh37 chr19: 260,912-58,956,888 , GRCh38.p12 chr19: 260,912-58,445,521 LENG8, SYDE1, 2408 more genes
    nsv3893926copy number variation1nstd102humanUncertain significance GRCh37 chr19: 46,192,402-46,603,824 , GRCh38.p12 chr19: 45,689,144-46,100,566 CCDC61, NANOS2, 19 more genes
    nsv3893153copy number variation1nstd102humanUncertain significance GRCh37 chr19: 46,268,077-46,307,777 , GRCh38.p12 chr19: 45,764,819-45,804,519 RSPH6A, MEIOSIN, 4 more genes
    nsv3891669copy number variation1nstd102humanPathogenic GRCh37 chr19: 43,013,365-47,241,534 , GRCh38.p12 chr19: 42,509,213-46,738,277 MIR320E, BCL3, 189 more genes
    nsv3215281copy number variation4nstd152human GRCh38 chr19: 45,763,465-45,783,390 , GRCh37.p13 chr19: 46,266,723-46,286,648 DMPK, DMWD, 3 more genes
    nsv2785402copy number variation1nstd132human NCBI36 chr19: 50,546,759-51,111,613 , GRCh37.p13 chr19: 45,854,919-46,419,773 , GRCh38.p12 chr19: 45,351,661-45,916,515 GIPR, GPR4, 33 more genes
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