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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3904753copy number variation1nstd102humanBenign GRCh37 chr18: 77,086,759-77,100,844 , GRCh38.p12 chr18: 79,326,759-79,340,844 ATP9B
    nsv3896389copy number variation1nstd102humanBenign GRCh37 chr18: 77,110,713-77,116,485 , GRCh38.p12 chr18: 79,350,713-79,356,485 ATP9B
    nsv3897971copy number variation1nstd102humanBenign GRCh37 chr18: 77,030,000-77,058,989 , GRCh38.p12 chr18: 79,270,000-79,298,989 ATP9B, LOC105372226
    nsv3906803copy number variation1nstd102humanBenign GRCh37 chr18: 77,052,242-77,063,702 , GRCh38.p12 chr18: 79,292,242-79,303,702 ATP9B, LOC105372226
    nsv3890887copy number variation1nstd102humanBenign GRCh37 chr18: 77,052,242-77,063,691 , GRCh38.p12 chr18: 79,292,242-79,303,691 ATP9B, LOC105372226
    nsv3907440copy number variation1nstd102humanBenign GRCh37 chr18: 77,057,765-77,065,954 , GRCh38.p12 chr18: 79,297,765-79,305,954 ATP9B, LOC105372226
    nsv3920893copy number variation1nstd102humanUncertain significance NCBI36 chr18: 74,878,921-75,074,959 , GRCh37.p13 chr18: 76,777,933-76,973,971 , GRCh38.p12 chr18: 79,017,933-79,213,971 ATP9B, LOC105372225
    nsv4729871copy number variation1nstd102humanLikely benign GRCh37 chr18: 76,976,938-77,133,402 , GRCh38.p12 chr18: 79,216,938-79,373,402 ATP9B, LOC105372226, 1 more genes
    nsv3904513copy number variation1nstd102humanUncertain significance GRCh37 chr18: 76,499,465-76,958,413 , GRCh38.p12 chr18: 78,739,465-79,198,413 ATP9B, LOC105372224, 3 more genes
    nsv3914859copy number variation1nstd102humanUncertain significance NCBI36 chr18: 75,015,527-75,303,978 , GRCh37.p13 chr18: 76,914,539-77,202,990 , GRCh38.p12 chr18: 79,154,539-79,442,990 ATP9B, LOC105372226, 2 more genes
    nsv3902831copy number variation1nstd102humanPathogenic GRCh37 chr18: 46,177,798-78,014,123 , GRCh38.p12 chr18: 48,651,427-80,256,240 ATP9B, LOC105372180, 370 more genes
    nsv3906152copy number variation1nstd102humanPathogenic GRCh37 chr18: 46,942,427-78,014,123 , GRCh38.p12 chr18: 49,416,057-80,256,240 ATP9B, RPL17P44, 360 more genes
    nsv3909519copy number variation1nstd102humanPathogenic GRCh37 chr18: 47,656,799-78,014,123 , GRCh38.p12 chr18: 50,130,429-80,256,240 ATP9B, LOC105372160, 339 more genes
    nsv3920508copy number variation1nstd102humanPathogenic GRCh38 chr18: 51,167,159-80,256,240 , GRCh37 chr18: 48,693,529-78,014,123 , NCBI36 chr18: 46,947,527-76,115,097 ATP9B, LOC105372152, 319 more genes
    nsv3916196copy number variation1nstd102humanPathogenic GRCh37 chr18: 48,716,799-78,010,032 , GRCh38 chr18: 51,190,429-80,252,149 , NCBI36 chr18: 46,970,797-76,111,023 ATP9B, LOC105372200, 319 more genes
    nsv4676105copy number variation1nstd102humanPathogenic GRCh37 chr18: 49,460,596-78,014,123 , GRCh38.p12 chr18: 51,934,226-80,256,240 ATP9B, MIR548AV, 310 more genes
    nsv3914571copy number variation1nstd102humanPathogenic GRCh37 chr18: 49,947,422-78,012,829 , NCBI36 chr18: 48,201,420-76,113,817 , GRCh38 chr18: 52,421,052-80,254,946 ATP9B, RPS2P6, 308 more genes
    nsv3918507copy number variation1nstd102humanPathogenic GRCh38 chr18: 53,865,057-80,252,149 , GRCh37 chr18: 51,391,427-78,010,032 , NCBI36 chr18: 49,645,425-76,111,023 ATP9B, NETO1, 303 more genes
    nsv6314216copy number variation1nstd102humanPathogenic GRCh37 chr18: 52,675,201-78,014,123 , GRCh38.p12 chr18: 55,007,970-80,256,240 ATP9B, RNA5SP461, 290 more genes
    nsv3899425copy number variation1nstd102humanPathogenic GRCh37 chr18: 52,802,515-78,015,180 , GRCh38.p12 chr18: 55,135,284-80,257,297 ATP9B, ZNF236-DT, 288 more genes
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