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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv1398070copy number variation1nstd102humanUncertain significance GRCh37 chr16: 31,123,271-31,153,163 , GRCh38.p12 chr16: 31,111,950-31,141,842 PRSS8, PRSS36, 2 more genes
    nsv4455315copy number variation1nstd102humanPathogenic GRCh37 chr16: 30,851,860-31,156,762 , GRCh38.p12 chr16: 30,840,539-31,145,441 PRSS8, LOC101928762, 20 more genes
    nsv3906108copy number variation1nstd102humanPathogenic GRCh37 chr16: 61,451-90,294,632 , GRCh38.p12 chr16: 11,451-90,228,224 PRSS8, CKLF, 1882 more genes
    nsv3904593copy number variation1nstd102humanPathogenic GRCh37 chr16: 69,193-90,274,381 , GRCh38.p12 chr16: 19,193-90,207,973 PRSS8, LOC100128079, 1879 more genes
    nsv3901410copy number variation1nstd102humanPathogenic GRCh37 chr16: 88,165-90,274,695 , GRCh38.p12 chr16: 38,165-90,208,287 PRSS8, LINC02175, 1877 more genes
    nsv3909417copy number variation1nstd102humanPathogenic GRCh37 chr16: 88,165-90,163,275 , GRCh38.p12 chr16: 38,165-90,096,867 PRSS8, PRSS53, 1868 more genes
    nsv3892266copy number variation2nstd102humanPathogenic GRCh37 chr16: 85,881-90,155,062 , GRCh38.p12 chr16: 35,881-90,088,654 PRSS8, FTLP14, 1868 more genes
    nsv4685985copy number variation1nstd102humanPathogenic GRCh37 chr16: 5,805,001-34,230,001 , GRCh38.p12 chr16: 5,755,000-34,995,630 PRSS8, LOC105371069, 654 more genes
    nsv3913895copy number variation1nstd102humanPathogenic NCBI36 chr16: 24,289,454-33,830,560 , GRCh37.p13 chr16: 24,381,953-33,923,059 , GRCh38.p12 chr16: 24,370,632-34,120,592 PRSS8, ITGAL, 310 more genes
    nsv3914248copy number variation1nstd102humanPathogenic GRCh37 chr16: 23,763,368-31,955,076 , GRCh38 chr16: 23,752,047-31,943,755 , NCBI36 chr16: 23,670,869-31,862,577 PRSS8, ZG16, 250 more genes
    nsv3918492copy number variation1nstd102humanPathogenic GRCh37 chr16: 30,703,233-35,147,508 , NCBI36 chr16: 30,610,734-35,005,009 , GRCh38 chr16: 30,691,912-36,160,463 PRSS8, KRBOX5P1, 213 more genes
    nsv3910351copy number variation1nstd102humanPathogenic GRCh38 chr16: 27,311,746-31,193,406 , NCBI36 chr16: 27,230,568-31,112,228 , GRCh37 chr16: 27,323,067-31,204,727 PRSS8, BCL7C, 171 more genes
    nsv3924250copy number variation1nstd102humanPathogenic NCBI36 chr16: 29,828,435-31,357,519 , GRCh37 chr16: 29,920,934-31,450,018 , GRCh38 chr16: 29,909,613-31,438,697 PRSS8, MIR4518, 95 more genes
    nsv4436312complex substitution1nstd102humanPathogenic GRCh38.p12 chr16: 1,230,041-33,908,091 , GRCh37 chr16: 1,280,042-33,710,558 PRSS8, ABAT, 876 more genes
    nsv3905126copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 28,826,162-34,375,007 , GRCh38.p12 chr16: 28,814,841-35,140,636 PRSS8, ALDOA, 255 more genes
    nsv3905250copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 30,943,854-31,171,177 , GRCh38.p12 chr16: 30,932,533-31,159,856 PRSS8, STX4, 13 more genes
    nsv3900609copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 30,952,806-31,177,641 , GRCh38.p12 chr16: 30,941,485-31,166,320 PRSS8, STX4, 13 more genes
    nsv3900464copy number variation1nstd102humanBenign GRCh37 chr16: 30,738,551-34,194,635 , GRCh38.p12 chr16: 30,727,230-34,960,264 PRSS8, ZNF646, 139 more genes
    nsv3888559copy number variation1nstd102humanUncertain significance GRCh37 chr16: 30,554,158-31,536,880 , GRCh38.p12 chr16: 30,542,837-31,525,559 PRSS8, SETD1A, 53 more genes
    nsv3895762copy number variation1nstd102humanUncertain significance GRCh37 chr16: 9,273,328-89,548,493 , GRCh38.p12 chr16: 9,179,471-89,482,085 PRSS8, HERC2P5, 1497 more genes
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