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Items: 1 to 20 of 126

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7053596inversion1nstd229human GRCh38 chr5: 85,730,857-88,063,519 , GRCh37.p13 chr5: 85,026,675-87,359,336 LOC100421863, RPL10AP9, 25 more genes
    nsv6775558copy number variation1nstd229human GRCh38 chr5: 86,155,296-86,359,706 , GRCh37.p13 chr5: 85,451,114-85,655,524 NBPF22P, LOC105379064
    nsv6775028copy number variation1nstd229human GRCh38 chr5: 86,288,527-86,291,472 , GRCh37.p13 chr5: 85,584,345-85,587,290 NBPF22P
    nsv6774884copy number variation1nstd229human GRCh38 chr5: 86,234,905-86,290,036 , GRCh37.p13 chr5: 85,530,723-85,585,854 NBPF22P
    nsv6773809copy number variation1nstd229human GRCh38 chr5: 85,331,847-86,332,180 , GRCh37.p13 chr5: 84,627,665-85,627,998 LOC645181, PTP4A1P4, 6 more genes
    nsv6772406copy number variation1nstd229human GRCh38 chr5: 86,283,001-86,312,300 , GRCh37.p13 chr5: 85,578,819-85,608,118 NBPF22P
    nsv6770884copy number variation1nstd229human GRCh38 chr5: 86,175,465-86,304,717 , GRCh37.p13 chr5: 85,471,283-85,600,535 NBPF22P
    nsv6763182copy number variation1nstd229human GRCh38 chr5: 86,293,371-86,299,888 , GRCh37.p13 chr5: 85,589,189-85,595,706 NBPF22P
    nsv6761992copy number variation1nstd229human GRCh38 chr5: 85,913,632-86,296,268 , GRCh37.p13 chr5: 85,209,450-85,592,086 LOC105379063, NBPF22P, 1 more genes
    nsv6760412copy number variation1nstd229human GRCh38 chr5: 86,127,035-87,005,434 , GRCh37.p13 chr5: 85,422,853-86,301,251 COX7C, LOC100421863, 6 more genes
    nsv6630810copy number variation1nstd224human GRCh37 chr5: 85,458,883-85,651,034 , GRCh38.p12 chr5: 86,163,065-86,355,216 LOC105379064, NBPF22P
    nsv6398989copy number variation1nstd223human GRCh38 chr5: 86,284,604-86,286,138 , GRCh37.p13 chr5: 85,580,422-85,581,956 NBPF22P
    nsv6398739copy number variation1nstd223human GRCh38 chr5: 83,701,679-87,055,970 , GRCh37.p13 chr5: 82,997,498-86,351,787 LOC645261, LOC105379061, 28 more genes
    nsv6313788copy number variation1nstd102humanPathogenic GRCh37 chr5: 82,185,951-90,110,454 , GRCh38.p12 chr5: 82,890,132-90,814,637 RASA1, HAPLN1, 82 more genes
    nsv6135438copy number variation1nstd213human GRCh37 chr5: 80,920,000-86,370,001 , GRCh38.p12 chr5: 81,624,181-87,074,184 COX7C, HAPLN1, 56 more genes
    nsv6135436copy number variation1nstd213human GRCh37 chr5: 70,260,000-91,630,001 , GRCh38.p12 chr5: 70,964,173-92,334,184 , ARSB, 300 more genes
    nsv6135200copy number variation1nstd213human GRCh37 chr5: 76,540,000-94,260,001 , GRCh38.p12 chr5: 77,244,175-94,924,296 ACTBP2, ARSB, 200 more genes
    nsv6065720insertion1nstd212human GRCh38 chr5: 86,293,772-86,293,772 , GRCh37.p13 chr5: 85,589,590-85,589,590 NBPF22P
    nsv5634005insertion1nstd207human GRCh38 chr5: 86,281,614-86,281,614 , GRCh37.p13 chr5: 85,577,432-85,577,432 NBPF22P
    nsv5307677copy number variation1nstd204human GRCh38.p13 chr5: 86,284,522-86,286,147 , GRCh37.p13 chr5: 85,580,340-85,581,965 NBPF22P
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