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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4360187copy number variation1nstd102humanPathogenic NCBI36 (hg18) chr16: 33,732-13,328,164 , GRCh37.p13 chr16: 93,732-13,420,663 , GRCh38.p12 chr16: 43,732-13,326,806 PRSS22, ADCY9, 429 more genes
    nsv4359806copy number variation1nstd102humanUncertain significance NCBI36 (hg18) chr16: 2,776,225-2,903,721 , GRCh37.p13 chr16: 2,836,224-2,963,720 , GRCh38.p12 chr16: 2,786,223-2,913,719 PRSS22, PRSS30P, 9 more genes
    nsv4359782copy number variation1nstd102humanPathogenic NCBI36 (hg18) chr16: 2,316,842-3,477,107 , GRCh37.p13 chr16: 2,376,841-3,537,106 , GRCh38.p12 chr16: 2,326,840-3,487,106 PRSS22, ATP6V0C, 101 more genes
    nsv4359423copy number variation1nstd102humanPathogenic NCBI36 (hg18) chr16: 36,766-3,204,624 , GRCh37.p13 chr16: 96,766-3,264,623 , GRCh38.p12 chr16: 46,766-3,214,623 PRSS22, ABCA3, 243 more genes
    nsv4358686copy number variation1nstd102humanPathogenic NCBI36 (hg18) chr16: 2,484,806-3,236,580 , GRCh37.p13 chr16: 2,544,805-3,296,579 , GRCh38.p12 chr16: 2,494,804-3,246,579 PRSS22, OR1F1, 74 more genes
    nsv4357857copy number variation1nstd102humanPathogenic NCBI36 (hg18) chr16: 36,766-4,237,187 , GRCh37.p13 chr16: 96,766-4,297,186 , GRCh38.p12 chr16: 46,766-4,247,185 PRSS22, DNASE1L2, 278 more genes
    nsv4355081copy number variation1nstd102humanPathogenic NCBI36 (hg18) chr16: 36,766-11,526,873 , GRCh37.p13 chr16: 96,766-11,619,372 , GRCh38.p12 chr16: 46,766-11,525,516 PRSS22, ARHGDIG, 399 more genes
    nsv4353402copy number variation1nstd102humanPathogenic NCBI36 (hg18) chr16: 2,707,954-4,031,022 , GRCh37.p13 chr16: 2,767,953-4,091,021 , GRCh38.p12 chr16: 2,717,952-4,041,020 PRSS22, ZNF205, 92 more genes
    nsv4353054copy number variation1nstd102humanPathogenic NCBI36 (hg18) chr16: 2,840,736-7,100,699 , GRCh37.p13 chr16: 2,900,735-7,160,698 , GRCh38.p12 chr16: 2,850,734-7,110,697 PRSS22, MEFV, 135 more genes
    nsv4351684copy number variation1nstd102humanPathogenic NCBI36 (hg18) chr16: 13,141-11,298,053 , GRCh37.p13 chr16: 73,141-11,390,552 , GRCh38.p12 chr16: 23,141-11,296,695 PRSS22, ARHGDIG, 395 more genes
    nsv4350748copy number variation1nstd102humanPathogenic GRCh37 (hg19) chr16: 716,662-15,836,961 , GRCh38.p12 chr16: 666,662-15,743,104 , NCBI36 (hg18) chr16: 656,663-15,744,462 PRSS22, ATP6V0C, 447 more genes
    nsv4349832copy number variation1nstd102humanPathogenic GRCh37 (hg19) chr16: 109,978-4,316,797 , GRCh38.p12 chr16: 59,980-4,266,796 , NCBI36 (hg18) chr16: 49,978-4,256,798 PRSS22, ABCA3, 278 more genes
    nsv4327481insertion1nstd166human GRCh37.p13 chr16: 2,901,654-2,901,663 , GRCh38.p12 chr16|NW_013171812.1: 31,120-31,140 , GRCh38.p12 chr16: 2,851,653-2,851,662 PRSS22
    nsv4234096copy number variation1nstd166human GRCh37.p13 chr16: 2,901,211-2,901,665 , GRCh38.p12 chr16: 2,851,210-2,851,664 , GRCh38.p12 chr16|NW_013171812.1: 30,676-31,142 PRSS22
    nsv4016585mobile element insertion1nstd166human GRCh37.p13 chr16: 2,438,151-17,257,935 , GRCh38.p12 chr16: 2,388,150-17,164,078 PRSS22, ABAT, 355 more genes
    nsv3966199insertion1nstd168human GRCh38 (hg38) chr16: 2,756,596-2,899,195 , GRCh37.p13 chr16: 2,806,597-2,949,196 PRSS22, PRSS21, 10 more genes
    nsv3912759copy number variation1nstd102humanUncertain significance NCBI36 (hg18) chr16: 2,728,569-2,874,237 , GRCh37.p13 chr16: 2,788,568-2,934,236 , GRCh38.p12 chr16: 2,738,567-2,884,235 PRSS22, ZG16B, 11 more genes
    nsv3909417copy number variation1nstd102humanPathogenic GRCh37 (hg19) chr16: 88,165-90,163,275 , GRCh38.p12 chr16: 38,165-90,096,867 , NCBI36 (hg18) chr16: 28,165-88,690,776 PRSS22, ADCY9, 1924 more genes
    nsv3908822copy number variation1nstd102humanPathogenic GRCh37 (hg19) chr16: 1,505,184-4,415,346 , GRCh38.p12 chr16: 1,455,183-4,365,345 , NCBI36 (hg18) chr16: 1,445,185-4,355,347 PRSS22, ADCY9, 190 more genes
    nsv3907093copy number variation1nstd102humanPathogenic GRCh37 (hg19) chr16: 97,133-5,122,974 , GRCh38.p12 chr16: 47,133-5,072,973 , NCBI36 (hg18) chr16: 37,133-5,062,975 PRSS22, ATP6V0C, 312 more genes
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