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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148091copy number variation1nstd102humanPathogenic GRCh37 chr16: 14,853,752-16,666,672 , GRCh38.p12 chr16: 14,759,895-16,572,815 RPL17P40, PKD1P3-NPIPA1, 54 more genes
    nsv7147704copy number variation1nstd232human GRCh37.p13 chr16: 14,967,879-14,967,954 , GRCh38.p12 chr16|NT_187607.1: 912,756-912,806 , GRCh38.p12 chr16: 14,874,022-14,874,097 NOMO1
    nsv7137121copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 14,819,740-16,364,041 , GRCh38.p12 chr16: 14,725,883-16,270,184 , GRCh38.p12 chr16|NT_187607.1: 266,171-1,928,187 ABCC6, ABCC1, 54 more genes
    nsv7099031copy number variation1nstd102humanUncertain significance GRCh38 chr16: 14,683,149-16,205,174 , GRCh37.p13 chr16: 14,777,006-16,299,031 LOC100288162, LOC105371096, 43 more genes
    nsv7098843copy number variation1nstd102humanLikely pathogenic GRCh38 chr16: 14,683,149-16,536,956 , GRCh37.p13 chr16: 14,777,006-16,630,813 ABCC6, ABCC1, 56 more genes
    nsv7093396copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 14,927,709-16,484,731 , GRCh38.p12 chr16: 14,833,852-16,390,874 ABCC6, ABCC1, 50 more genes
    nsv7076079inversion1nstd229human GRCh38 chr16: 9,015,595-14,846,246 , GRCh37.p13 chr16: 9,109,452-14,940,103 LOC105371093, RNU6-633P, 100 more genes
    nsv7073405inversion1nstd229human GRCh38 chr16: 14,540,157-14,993,130 , GRCh37.p13 chr16: 14,634,014-15,086,987 LOC100652777, NPIPA1, 20 more genes
    nsv7072871inversion1nstd229human GRCh38 chr16: 14,843,584-14,843,608 , GRCh37.p13 chr16: 14,937,441-14,937,465 NOMO1
    nsv7068744inversion1nstd229human GRCh38 chr16: 14,595,692-15,383,928 , GRCh37.p13 chr16: 14,689,549-15,477,785 PKD1P6, NPIPA5, 32 more genes
    nsv7067918inversion1nstd229human GRCh38 chr16: 14,867,200-18,528,889 , GRCh37.p13 chr16: 14,961,057-18,540,211 NPIPA1, NDE1, 80 more genes
    nsv7065280inversion1nstd229human GRCh38 chr16: 14,489,001-15,167,857 , GRCh37.p13 chr16: 14,582,858-15,261,714 NPIPA2, PARN, 31 more genes
    nsv6637929copy number variation1nstd102humanPathogenic GRCh37 chr16: 14,780,544-16,330,627 , GRCh38.p12 chr16: 14,686,687-16,236,770 , GRCh38.p12 chr16|NT_187607.1: 259,546-1,894,768 LOC102724984, ABCC6P2, 54 more genes
    nsv6637792copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 14,925,995-16,309,165 , GRCh38.p12 chr16: 14,832,138-16,215,308 , GRCh38.p12 chr16|NT_187607.1: 531,831-1,873,305 ABCC6, ABCC1, 49 more genes
    nsv6637442copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 14,365,745-17,052,798 , GRCh38.p12 chr16: 14,271,888-16,958,941 ABCC6, ABCC1, 69 more genes
    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
    nsv6623555copy number variation1nstd224human GRCh37 chr16: 15,103,681-16,299,148 , GRCh38.p12 chr16: 15,009,824-16,205,291 , GRCh38.p12 chr16|NT_187607.1: 849,174-1,863,289 MARF1, PDXDC1, 32 more genes
    nsv6623554copy number variation1nstd224human GRCh37 chr16: 15,098,128-16,291,983 , GRCh38.p12 chr16: 15,004,271-16,198,126 , GRCh38.p12 chr16|NT_187607.1: 843,618-1,856,122 ABCC1, MARF1, 32 more genes
    nsv6623553copy number variation1nstd224human GRCh37 chr16: 14,975,292-15,188,025 , GRCh38.p12 chr16: 14,881,435-15,094,168 NPIPA1, RRN3, 15 more genes
    nsv6623405copy number variation1nstd224human GRCh37 chr16: 15,122,745-16,301,530 , GRCh38.p12 chr16: 15,028,888-16,207,673 , GRCh38.p12 chr16|NT_187607.1: 868,233-1,865,671 MPV17L, ABCC6P1, 32 more genes
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