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Items: 1 to 20 of 76

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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
    nsv5533058copy number variation1nstd206human GRCh38 chr19: 46,021,729-46,021,817 , GRCh37.p13 chr19: 46,524,987-46,525,075 PGLYRP1, LOC105372421
    nsv5020739copy number variation1nstd200human GRCh38 chr19: 46,021,729-46,021,817 , GRCh37.p13 chr19: 46,524,987-46,525,075 PGLYRP1, LOC105372421
    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
    nsv4457603copy number variation1nstd102humanUncertain significance GRCh37 chr19: 46,495,215-46,552,877 , GRCh38.p12 chr19: 45,991,957-46,049,619 CCDC61, PGLYRP1, 3 more genes
    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
    nsv4261057copy number variation1nstd166human GRCh37.p13 chr19: 46,518,342-46,521,627 , GRCh38.p12 chr19: 46,015,084-46,018,369 PGLYRP1, CCDC61, 1 more genes
    nsv4260444copy number variation1nstd166human GRCh37.p13 chr19: 46,524,987-46,525,075 , GRCh38.p12 chr19: 46,021,729-46,021,817 PGLYRP1, LOC105372421
    nsv3971281copy number variation1nstd168human GRCh38 chr19: 46,000,862-46,046,699 , GRCh37.p13 chr19: 46,504,120-46,549,957 PGLYRP1, IGFL4, 3 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
    nsv3903092copy number variation2nstd102humanPathogenic GRCh37 chr19: 260,912-58,956,888 , GRCh38.p12 chr19: 260,912-58,445,521 LENG8, SYDE1, 2408 more genes
    nsv3900160copy number variation1nstd102humanLikely pathogenic GRCh37 chr19: 46,404,248-48,488,721 , GRCh38.p12 chr19: 45,900,990-47,985,464 C5AR1, CALM3, 84 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
    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
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