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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3893532copy number variation1nstd102humanBenign GRCh37 chr16: 80,975,540-81,027,685 , GRCh38.p12 chr16: 80,941,643-80,994,080 CMC2
    nsv3913814copy number variation1nstd102humanUncertain significance NCBI36 chr16: 79,450,426-79,579,474 , GRCh37.p13 chr16: 80,892,925-81,021,973 , GRCh38.p12 chr16: 80,859,028-80,988,368 CMC2, ARLNC1
    nsv6637496copy number variation1nstd102humanUncertain significance GRCh37 chr16: 80,975,918-81,049,683 , GRCh38.p12 chr16: 80,942,021-81,016,078 CMC2, CENPN
    nsv3906220copy number variation1nstd102humanBenign GRCh37 chr16: 80,982,897-81,076,970 , GRCh38.p12 chr16: 80,949,000-81,043,365 CMC2, ATMIN, 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 CMC2, NECAB2, 219 more genes
    nsv3918168copy number variation1nstd102humanPathogenic NCBI36 chr16: 71,640,867-81,167,432 , GRCh38 chr16: 73,049,467-82,576,326 , GRCh37 chr16: 73,083,366-82,609,931 CMC2, BCAR1, 125 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 CMC2, RPL10AP12, 146 more genes
    nsv3916915copy number variation1nstd102humanPathogenic NCBI36 chr16: 77,381,848-81,846,527 , GRCh38 chr16: 78,790,450-83,255,421 , GRCh37 chr16: 78,824,347-83,289,026 CMC2, LOC100419639, 50 more genes
    nsv3923041copy number variation1nstd102humanPathogenic GRCh38 chr16: 79,455,147-81,109,328 , NCBI36 chr16: 78,046,545-79,700,434 , GRCh37 chr16: 79,489,044-81,142,933 CMC2, CENPN, 19 more genes
    nsv3884480copy number variation1nstd102humanPathogenic GRCh37 chr16: 80,623,263-81,411,221 , GRCh38.p12 chr16: 80,589,366-81,377,616 CMC2, C16orf46, 11 more genes
    nsv3906108copy number variation1nstd102humanPathogenic GRCh37 chr16: 61,451-90,294,632 , GRCh38.p12 chr16: 11,451-90,228,224 CMC2, CKLF, 1882 more genes
    nsv3904593copy number variation1nstd102humanPathogenic GRCh37 chr16: 69,193-90,274,381 , GRCh38.p12 chr16: 19,193-90,207,973 CMC2, LOC100128079, 1879 more genes
    nsv3901410copy number variation1nstd102humanPathogenic GRCh37 chr16: 88,165-90,274,695 , GRCh38.p12 chr16: 38,165-90,208,287 CMC2, LINC02175, 1877 more genes
    nsv3909417copy number variation1nstd102humanPathogenic GRCh37 chr16: 88,165-90,163,275 , GRCh38.p12 chr16: 38,165-90,096,867 CMC2, PRSS53, 1868 more genes
    nsv3892266copy number variation2nstd102humanPathogenic GRCh37 chr16: 85,881-90,155,062 , GRCh38.p12 chr16: 35,881-90,088,654 CMC2, 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 CMC2, LOC105371237, 985 more genes
    nsv6314755copy number variation1nstd102humanPathogenic GRCh37 chr16: 46,503,968-90,155,062 , GRCh38.p12 chr16: 46,470,056-90,088,654 CMC2, ATMIN, 826 more genes
    nsv3915506copy number variation1nstd102humanPathogenic NCBI36 chr16: 51,490,596-88,682,563 , GRCh38 chr16: 52,899,183-90,088,654 , GRCh37 chr16: 52,933,095-90,155,062 CMC2, CFAP69P1, 716 more genes
    nsv3891306copy number variation1nstd102humanPathogenic GRCh37 chr16: 57,051,473-89,797,669 , GRCh38.p12 chr16: 57,017,561-89,731,261 CMC2, LOC107984894, 613 more genes
    nsv3913913copy number variation1nstd102humanPathogenic NCBI36 chr16: 62,980,782-88,675,894 , GRCh38 chr16: 64,389,378-90,081,985 , GRCh37 chr16: 64,423,281-90,148,393 CMC2, ATP5F1AP3, 534 more genes
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