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Items: 1 to 20 of 139

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6309428copy number variation1nstd102humanPathogenic GRCh37 chr13: 100,861,576-100,955,262 , GRCh38.p12 chr13: 100,209,322-100,303,008 PCCA
    nsv5672648copy number variation1nstd102humanPathogenic GRCh37 chr13: 101,020,716-101,101,569 , GRCh38.p12 chr13: 100,368,462-100,449,315 PCCA
    nsv4682366copy number variation1nstd102humanPathogenic GRCh37 chr13: 100,861,576-100,888,142 , GRCh38.p12 chr13: 100,209,322-100,235,888 PCCA
    nsv7094160copy number variation1nstd102humanPathogenic GRCh37 chr13: 100,920,933-100,925,610 , GRCh38.p12 chr13: 100,268,679-100,273,356 PCCA
    nsv6309525copy number variation1nstd102humanPathogenic GRCh37 chr13: 100,807,223-100,809,604 , GRCh38.p12 chr13: 100,154,969-100,157,350 PCCA
    nsv4451804copy number variation1nstd102humanPathogenic GRCh38 chr13: 100,111,831-100,112,071 , GRCh37 chr13: 100,764,085-100,764,325 PCCA
    nsv6309494copy number variation1nstd102humanPathogenic GRCh37 chr13: 100,925,430-100,925,620 , GRCh38.p12 chr13: 100,273,176-100,273,366 PCCA
    nsv7094233copy number variation1nstd102humanPathogenic GRCh37 chr13: 101,167,661-101,167,841 , GRCh38.p12 chr13: 100,515,407-100,515,587 PCCA
    nsv6309497copy number variation1nstd102humanPathogenic GRCh37 chr13: 101,179,909-101,180,026 , GRCh38.p12 chr13: 100,527,655-100,527,772 PCCA
    nsv4682954copy number variation1nstd102humanPathogenic GRCh37 chr13: 100,920,933-100,921,047 , GRCh38.p12 chr13: 100,268,679-100,268,793 PCCA
    nsv4682519copy number variation1nstd102humanLikely pathogenic GRCh37 chr13: 100,807,223-100,925,610 , GRCh38.p12 chr13: 100,154,969-100,273,356 PCCA
    nsv6309330copy number variation1nstd102humanLikely pathogenic GRCh37 chr13: 100,809,575-100,810,037 , GRCh38 chr13: 100,157,321-100,157,783 PCCA
    nsv4683805copy number variation1nstd102humanLikely pathogenic GRCh37 chr13: 101,077,867-101,078,005 , GRCh38.p12 chr13: 100,425,613-100,425,751 PCCA
    nsv5672797copy number variation1nstd102humanLikely pathogenic GRCh37 chr13: 100,953,694-100,962,182 , GRCh38.p12 chr13: 100,301,440-100,309,928 PCCA
    nsv7093987copy number variation1nstd102humanLikely pathogenic GRCh37 chr13: 100,953,704-100,962,172 , GRCh38.p12 chr13: 100,301,450-100,309,918 PCCA
    nsv3906527copy number variation1nstd102humanUncertain significance GRCh37 chr13: 100,825,782-100,942,854 , GRCh38.p12 chr13: 100,173,528-100,290,600 PCCA
    nsv5380906copy number variation1nstd102humanUncertain significance GRCh37 chr13: 100,861,566-100,861,737 , GRCh38.p12 chr13: 100,209,312-100,209,483 PCCA
    nsv7094063copy number variation1nstd102humanUncertain significance GRCh37 chr13: 101,077,867-101,101,579 , GRCh38.p12 chr13: 100,425,613-100,449,325 PCCA
    nsv6309524copy number variation1nstd102humanUncertain significance GRCh37 chr13: 100,807,213-100,809,614 , GRCh38.p12 chr13: 100,154,959-100,157,360 PCCA
    nsv7094158copy number variation1nstd102humanPathogenic GRCh37 chr13: 100,909,829-101,101,579 , GRCh38.p12 chr13: 100,257,575-100,449,325 PCCA, LOC105370335
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