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Items: 1 to 20 of 246

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv3994462copy number variation1estd218human GRCh38.p12 chr16: 15,037,219-15,131,526 , GRCh37 chr16: 15,131,076-15,225,383 , GRCh38.p12 chr16|NT_187607.1: 533,729-632,468 PDXDC1, RRN3, 5 more genes
    esv3993649copy number variation1estd218human GRCh37 chr16: 15,092,778-16,291,983 , GRCh38.p12 chr16: 14,998,921-16,198,126 , GRCh38.p12 chr16|NT_187607.1: 838,268-1,856,122 , ABCC6, 34 more genes
    nsv2768204copy-neutral loss of heterozygosity1nstd125human GRCh38.p12 chr16: 569,967-35,986,173 , GRCh37 chr16: 619,967-35,220,544 , ABAT, 1043 more genes
    esv3876840copy number variation19estd219human GRCh38.p12 chr16: 15,130,224-15,205,817 , GRCh37 chr16: 15,224,081-15,299,674 , GRCh38.p12 chr16|NT_187607.1: 456,711-535,031 PDXDC1, PKD1P6, 5 more genes
    esv3986451copy number variation2estd229human GRCh37 chr16: 15,200,101-15,205,950 , GRCh38.p12 chr16: 15,106,244-15,112,093 PDXDC1, LOC100505915, 2 more genes
    nsv2760583copy number variation1nstd130human GRCh37 chr16: 15,048,643-16,290,495 , GRCh38.p12 chr16: 14,954,786-16,196,638 , GRCh38.p12 chr16|NT_187607.1: 794,120-1,854,634 , MIR3180-4, 35 more genes
    nsv2758718copy number variation1nstd130human GRCh37 chr16: 15,126,890-16,292,323 , GRCh38.p12 chr16: 15,033,033-16,198,466 , GRCh38.p12 chr16|NT_187607.1: 1,015,619-1,856,462 , NTAN1, 27 more genes
    nsv2745760copy number variation1nstd130human NCBI36 chr16: 15,032,942-15,192,528 , GRCh37.p13 chr16: 15,125,441-15,285,027 , GRCh38.p12 chr16: 15,031,584-15,191,170 , GRCh38.p12 chr16|NT_187607.1: 471,358-638,105 NTAN1, LOC100505915, 9 more genes
    nsv2745521copy number variation1nstd130human NCBI36 chr16: 15,032,942-16,538,314 , GRCh37.p13 chr16: 15,125,441-16,630,813 , GRCh38.p12 chr16: 15,031,584-16,536,956 , GRCh38.p12 chr16|NT_187607.1: 1,015,619-2,198,016 , NPIPP1, 41 more genes
    nsv2744330copy number variation1nstd130human NCBI36 chr16: 15,012,308-16,199,484 , GRCh37.p13 chr16: 15,104,807-16,291,983 , GRCh38.p12 chr16: 15,010,950-16,198,126 , GRCh38.p12 chr16|NT_187607.1: 850,300-1,856,122 , MIR484, 33 more genes
    nsv2740423copy number variation1nstd130human NCBI36 chr16: 14,805,479-16,199,484 , GRCh37.p13 chr16: 14,897,978-16,291,983 , GRCh38.p12 chr16: 14,804,121-16,198,126 , GRCh38.p12 chr16|NT_187607.1: 337,847-1,856,122 , LOC100288162, 52 more genes
    nsv2737396copy number variation1nstd130human NCBI36 chr16: 14,667,269-16,197,033 , GRCh37.p13 chr16: 14,759,768-16,289,532 , GRCh38.p12 chr16: 14,665,911-16,195,675 , GRCh38.p12 chr16|NT_187607.1: 238,769-1,853,670 , MIR6506, 59 more genes
    nsv2737176copy number variation1nstd130human NCBI36 chr16: 15,033,128-16,197,227 , GRCh37.p13 chr16: 15,125,627-16,289,726 , GRCh38.p12 chr16: 15,031,770-16,195,869 , GRCh38.p12 chr16|NT_187607.1: 1,015,619-1,853,864 , MIR484, 27 more genes
    nsv2735614copy number variation1nstd130human NCBI36 chr16: 14,991,891-16,199,484 , GRCh37.p13 chr16: 15,084,390-16,291,983 , GRCh38.p12 chr16: 14,990,533-16,198,126 , GRCh38.p12 chr16|NT_187607.1: 829,885-1,856,122 , NPIPA5, 35 more genes
    nsv2729197copy number variation7nstd130human NCBI36 chr16: 15,032,942-16,197,033 , GRCh37.p13 chr16: 15,125,441-16,289,532 , GRCh38.p12 chr16: 15,031,584-16,195,675 , GRCh38.p12 chr16|NT_187607.1: 1,015,619-1,853,670 , NPIPA5, 27 more genes
    nsv1817669short tandem repeat4nstd128human GRCh37 chr16: 15,204,006-15,204,018 , GRCh38.p12 chr16: 15,110,149-15,110,161 PKD1P6-NPIPP1, NPIPP1, 1 more genes
    nsv1398399copy number variation1nstd102humanUncertain significance GRCh37 chr16: 1,279,324-31,926,800 , GRCh38.p12 chr16: 1,229,323-31,915,479 FLYWCH2, LOC102723708, 817 more genes
    nsv1398297copy number variation1nstd102humanPathogenic GRCh37 chr16: 102,839-28,327,676 , GRCh38.p12 chr16: 52,839-28,316,355 BMERB1, LOC105371094, 701 more genes
    nsv1398209copy number variation1nstd102humanUncertain significance GRCh37 chr16: 1,274,615-19,073,133 , GRCh38.p12 chr16: 1,224,615-19,061,811 HAPSTR1, MTND4P34, 456 more genes
    nsv1389088copy number variation1nstd122human NCBI36 chr16: 14,991,776-15,406,558 , GRCh37.p13 chr16: 15,084,275-15,499,057 , GRCh38.p12 chr16: 14,990,418-15,405,200 , NTAN1, 15 more genes
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