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Items: 1 to 20 of 678

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148099copy number variation1nstd102humanPathogenic GRCh37 chr16: 15,125,542-16,388,672 , GRCh38.p12 chr16: 15,031,685-16,294,815 , GRCh38.p12 chr16|NT_187607.1: 1,015,619-1,952,820 LOC100505915, ABCC1, 28 more genes
    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
    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
    nsv7076232inversion1nstd229human GRCh38 chr16: 14,972,012-15,457,502 , GRCh37.p13 chr16: 15,065,869-15,551,359 MIR3180-4, LOC105371097, 14 more genes
    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
    nsv7067385inversion1nstd229human GRCh38 chr16: 15,051,408-15,524,165 , GRCh37.p13 chr16: 15,145,265-15,618,022 LOC105371096, MPV17L, 13 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
    nsv6967723copy number variation1nstd229human GRCh38 chr16: 15,074,345-15,082,691 , GRCh37.p13 chr16: 15,168,202-15,176,548 RRN3, PDXDC1
    nsv6967585copy number variation1nstd229human GRCh38 chr16: 14,928,133-16,326,551 , GRCh37.p13 chr16: 15,021,990-16,420,408 NPIPA5, PKD1P6, 39 more genes
    nsv6964784copy number variation1nstd229human GRCh38 chr16: 15,087,799-15,091,792 , GRCh37.p13 chr16: 15,181,656-15,185,649 RRN3, PDXDC1
    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
    nsv6623558copy number variation1nstd224human GRCh37 chr16: 15,125,627-15,844,182 , GRCh38.p12 chr16: 15,031,770-15,750,325 , GRCh38.p12 chr16|NT_187607.1: 1,015,619-1,408,336 MYH11, PKD1P6, 18 more genes
    nsv6623557copy number variation1nstd224human GRCh37 chr16: 15,125,441-15,235,820 , GRCh38.p12 chr16: 15,031,584-15,141,963 , GRCh38.p12 chr16|NT_187607.1: 520,541-638,105 PDXDC1, RRN3, 6 more genes
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