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Items: 1 to 20 of 23

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3905855copy number variation1nstd102humanPathogenic GRCh37 chr16: 21,596,299-30,399,167 , GRCh38.p12 chr16: 21,584,978-30,387,846 CD2BP2, LOC107984874, 217 more genes
    nsv3911651copy number variation1nstd102humanPathogenic NCBI36 chr16: 29,500,284-30,610,734 , GRCh38 chr16: 29,581,462-30,691,912 , GRCh37 chr16: 29,592,783-30,703,233 CD2BP2, PPP4C, 71 more genes
    nsv3906108copy number variation1nstd102humanPathogenic GRCh37 chr16: 61,451-90,294,632 , GRCh38.p12 chr16: 11,451-90,228,224 CD2BP2, CKLF, 1882 more genes
    nsv3904593copy number variation1nstd102humanPathogenic GRCh37 chr16: 69,193-90,274,381 , GRCh38.p12 chr16: 19,193-90,207,973 CD2BP2, LOC100128079, 1879 more genes
    nsv3901410copy number variation1nstd102humanPathogenic GRCh37 chr16: 88,165-90,274,695 , GRCh38.p12 chr16: 38,165-90,208,287 CD2BP2, LINC02175, 1877 more genes
    nsv3909417copy number variation1nstd102humanPathogenic GRCh37 chr16: 88,165-90,163,275 , GRCh38.p12 chr16: 38,165-90,096,867 CD2BP2, PRSS53, 1868 more genes
    nsv3892266copy number variation2nstd102humanPathogenic GRCh37 chr16: 85,881-90,155,062 , GRCh38.p12 chr16: 35,881-90,088,654 CD2BP2, FTLP14, 1868 more genes
    nsv4685985copy number variation1nstd102humanPathogenic GRCh37 chr16: 5,805,001-34,230,001 , GRCh38.p12 chr16: 5,755,000-34,995,630 CD2BP2, LOC105371069, 654 more genes
    nsv6637429copy number variation1nstd102humanPathogenic GRCh37 chr16: 4,380,767-30,445,350 , GRCh38.p12 chr16: 4,330,766-30,434,029 CD2BP2, MIR6511B2, 535 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 CD2BP2, 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 CD2BP2, ZG16, 250 more genes
    nsv3916220copy number variation1nstd102humanPathogenic GRCh37 chr16: 23,059,290-30,643,566 , NCBI36 chr16: 22,966,791-30,551,067 , GRCh38 chr16: 23,047,969-30,632,245 CD2BP2, MIR548W, 196 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 CD2BP2, 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 CD2BP2, MIR4518, 95 more genes
    nsv6290347copy number variation1nstd102humanPathogenic GRCh37 chr16: 29,808,153-30,750,270 , GRCh38.p12 chr16: 29,796,832-30,738,949 CD2BP2, SULT1A3, 65 more genes
    nsv3922448copy number variation1nstd102humanPathogenic GRCh38 chr16: 29,892,937-30,433,124 , NCBI36 chr16: 29,811,759-30,351,946 , GRCh37 chr16: 29,904,258-30,444,445 CD2BP2, ASPHD1, 37 more genes
    nsv4436312complex substitution1nstd102humanPathogenic GRCh38.p12 chr16: 1,230,041-33,908,091 , GRCh37 chr16: 1,280,042-33,710,558 CD2BP2, 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 CD2BP2, ALDOA, 255 more genes
    nsv6290281copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 29,974,415-30,596,982 , GRCh38.p12 chr16: 29,963,094-30,585,661 CD2BP2, ALDOA, 44 more genes
    nsv3895762copy number variation1nstd102humanUncertain significance GRCh37 chr16: 9,273,328-89,548,493 , GRCh38.p12 chr16: 9,179,471-89,482,085 CD2BP2, HERC2P5, 1497 more genes
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