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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3904877copy number variation1nstd102humanLikely benign GRCh37 chr16: 84,365,725-84,616,225 , GRCh38.p12 chr16: 84,332,119-84,582,619 MEAK7, ATP2C2-AS1, 2 more genes
    nsv3894292copy number variation1nstd102humanBenign GRCh37 chr16: 84,440,081-84,524,260 , GRCh38.p12 chr16: 84,406,475-84,490,654 MEAK7, ATP2C2-AS1, 1 more genes
    nsv3893023copy number variation1nstd102humanBenign GRCh37 chr16: 84,433,034-84,544,608 , GRCh38.p12 chr16: 84,399,428-84,511,002 MEAK7, ATP2C2-AS1, 1 more genes
    nsv4456510copy number variation1nstd102humanUncertain significance GRCh37 chr16: 84,423,471-84,530,235 , GRCh38.p12 chr16: 84,389,865-84,496,629 MEAK7, ATP2C2-AS1, 1 more genes
    nsv4457124copy number variation1nstd102humanUncertain significance GRCh37 chr16: 84,471,514-84,510,221 , GRCh38.p12 chr16: 84,437,908-84,476,615 MEAK7, ATP2C2-AS1, 1 more genes
    nsv4674986copy number variation1nstd102humanUncertain significance GRCh37 chr16: 84,420,340-84,664,139 , GRCh38.p12 chr16: 84,386,734-84,630,533 MEAK7, ATP2C2-AS1, 2 more genes
    nsv3921095copy number variation1nstd102humanPathogenic NCBI36 chr16: 69,005,977-83,499,227 , GRCh38 chr16: 70,414,573-84,908,120 , GRCh37 chr16: 70,448,476-84,941,726 MEAK7, NECAB2, 219 more genes
    nsv3919844copy number variation1nstd102humanPathogenic GRCh38 chr16: 78,704,275-87,819,342 , GRCh37 chr16: 78,738,172-87,852,948 , NCBI36 chr16: 77,295,673-86,410,449 MEAK7, RPL10AP12, 146 more genes
    nsv3917609copy number variation1nstd102humanPathogenic NCBI36 chr16: 80,344,868-84,305,898 , GRCh37 chr16: 81,787,367-85,748,397 , GRCh38 chr16: 81,753,762-85,714,791 MEAK7, LOC105371376, 63 more genes
    nsv3911104copy number variation1nstd102humanPathogenic GRCh37 chr16: 83,912,597-87,257,444 , GRCh38 chr16: 83,878,992-87,223,838 , NCBI36 chr16: 82,470,098-85,814,945 MEAK7, LOC101928557, 75 more genes
    nsv3922440copy number variation1nstd102humanPathogenic NCBI36 chr16: 82,278,756-84,664,347 , GRCh37 chr16: 83,721,255-86,106,846 , GRCh38 chr16: 83,687,650-86,073,240 MEAK7, LOC123862, 58 more genes
    nsv3922490copy number variation1nstd102humanPathogenic GRCh38 chr16: 83,016,872-85,087,809 , GRCh37 chr16: 83,050,477-85,121,415 , NCBI36 chr16: 81,607,978-83,678,916 MEAK7, MBTPS1, 33 more genes
    nsv3922339copy number variation1nstd102humanPathogenic GRCh37 chr16: 83,432,665-84,941,726 , GRCh38 chr16: 83,399,060-84,908,120 , NCBI36 chr16: 81,990,166-83,499,227 MEAK7, LOC648774, 28 more genes
    nsv3906108copy number variation1nstd102humanPathogenic GRCh37 chr16: 61,451-90,294,632 , GRCh38.p12 chr16: 11,451-90,228,224 MEAK7, CKLF, 1882 more genes
    nsv3904593copy number variation1nstd102humanPathogenic GRCh37 chr16: 69,193-90,274,381 , GRCh38.p12 chr16: 19,193-90,207,973 MEAK7, LOC100128079, 1879 more genes
    nsv3901410copy number variation1nstd102humanPathogenic GRCh37 chr16: 88,165-90,274,695 , GRCh38.p12 chr16: 38,165-90,208,287 MEAK7, LINC02175, 1877 more genes
    nsv3909417copy number variation1nstd102humanPathogenic GRCh37 chr16: 88,165-90,163,275 , GRCh38.p12 chr16: 38,165-90,096,867 MEAK7, PRSS53, 1868 more genes
    nsv3892266copy number variation2nstd102humanPathogenic GRCh37 chr16: 85,881-90,155,062 , GRCh38.p12 chr16: 35,881-90,088,654 MEAK7, FTLP14, 1868 more genes
    nsv3921269copy number variation1nstd102humanPathogenic NCBI36 chr16: 31,893,599-88,822,254 , GRCh37.p13 chr16: 31,986,098-90,294,753 , GRCh38.p12 chr16: 31,974,777-90,228,345 MEAK7, LOC105371237, 985 more genes
    nsv6314755copy number variation1nstd102humanPathogenic GRCh37 chr16: 46,503,968-90,155,062 , GRCh38.p12 chr16: 46,470,056-90,088,654 MEAK7, ATMIN, 826 more genes
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