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Items: 1 to 20 of 235

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7077306inversion1nstd229human GRCh38 chr16: 20,312,926-20,501,990 , GRCh37.p13 chr16: 20,324,248-20,513,312 GP2, ACSM5, 4 more genes
    nsv7076939inversion1nstd229human GRCh38 chr16: 15,569,413-22,730,334 , GRCh37.p13 chr16: 15,663,270-22,741,655 ACSM5P1, RNU6-213P, 154 more genes
    nsv7076413inversion1nstd229human GRCh38 chr16: 20,420,290-20,603,506 , GRCh37.p13 chr16: 20,431,612-20,614,828 ACSM5P1, LOC105371119, 5 more genes
    nsv7068933inversion1nstd229human GRCh38 chr16: 20,325,688-20,609,015 , GRCh37.p13 chr16: 20,337,010-20,620,337 GP2, PDILT, 9 more genes
    nsv7067405inversion1nstd229human GRCh38 chr16: 20,431,947-20,591,664 , GRCh37.p13 chr16: 20,443,269-20,602,986 LOC105371119, ACSM5, 4 more genes
    nsv7066115inversion1nstd229human GRCh38 chr16: 20,421,589-20,425,084 , GRCh37.p13 chr16: 20,432,911-20,436,406 ACSM5
    nsv7065706inversion1nstd229human GRCh38 chr16: 20,421,527-20,598,188 , GRCh37.p13 chr16: 20,432,849-20,609,510 ACSM2B, LOC105371119, 4 more genes
    nsv7064769inversion1nstd229human GRCh38 chr16: 20,438,962-20,587,254 , GRCh37.p13 chr16: 20,450,284-20,598,576 ACSM5, LOC112267906, 4 more genes
    nsv7061433inversion1nstd229human GRCh38 chr16: 19,893,387-21,501,582 , GRCh37.p13 chr16: 19,904,709-21,512,903 CRYM, SNX29P1, 38 more genes
    nsv7059443inversion1nstd229human GRCh38 chr16: 20,327,016-20,536,162 , GRCh37.p13 chr16: 20,338,338-20,547,484 ACSM2A, PDILT, 5 more genes
    nsv7059273inversion1nstd229human GRCh38 chr16: 20,380,547-20,567,019 , GRCh37.p13 chr16: 20,391,869-20,578,341 ACSM5, PDILT, 3 more genes
    nsv7059025inversion1nstd229human GRCh38 chr16: 20,379,226-20,476,570 , GRCh37.p13 chr16: 20,390,548-20,487,892 ACSM5, ACSM2A, 2 more genes
    nsv7058800inversion1nstd229human GRCh38 chr16: 20,415,880-20,534,814 , GRCh37.p13 chr16: 20,427,202-20,546,136 LOC105371119, ACSM5, 2 more genes
    nsv6994327copy number variation1nstd229human GRCh38 chr16: 20,439,755-20,440,697 , GRCh37.p13 chr16: 20,451,077-20,452,019 LOC105371119, ACSM5
    nsv6993374copy number variation1nstd229human GRCh38 chr16: 20,438,201-20,439,000 , GRCh37.p13 chr16: 20,449,523-20,450,322 ACSM5
    nsv6991214copy number variation1nstd229human GRCh38 chr16: 20,408,381-20,408,944 , GRCh37.p13 chr16: 20,419,703-20,420,266 ACSM5
    nsv6987107copy number variation1nstd229human GRCh38 chr16: 20,438,001-20,439,100 , GRCh37.p13 chr16: 20,449,323-20,450,422 ACSM5
    nsv6981207copy number variation1nstd229human GRCh38 chr16: 20,439,797-20,440,656 , GRCh37.p13 chr16: 20,451,119-20,451,978 LOC105371119, ACSM5
    nsv6978449copy number variation1nstd229human GRCh38 chr16: 20,421,527-20,425,444 , GRCh37.p13 chr16: 20,432,849-20,436,766 ACSM5
    nsv6637429copy number variation1nstd102humanPathogenic GRCh37 chr16: 4,380,767-30,445,350 , GRCh38.p12 chr16: 4,330,766-30,434,029 MIR6511B2, ACSM5, 535 more genes
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