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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4729126copy number variation1nstd102humanUncertain significance GRCh37 chr11: 125,777,055-125,838,856 , GRCh38.p12 chr11: 125,907,160-125,968,961 DDX25, CDON, 1 more genes
    nsv4455408copy number variation1nstd102humanUncertain significance GRCh37 chr11: 125,777,055-125,838,831 , GRCh38.p12 chr11: 125,907,160-125,968,936 DDX25, CDON, 1 more genes
    nsv6291027copy number variation1nstd102humanUncertain significance GRCh37 chr11: 125,778,528-125,836,238 , GRCh38.p12 chr11: 125,908,633-125,966,343 DDX25, VSIG10L2, 1 more genes
    nsv3901131copy number variation1nstd102humanUncertain significance GRCh37 chr11: 125,781,319-125,827,813 , GRCh38.p12 chr11: 125,911,424-125,957,918 DDX25, VSIG10L2, 1 more genes
    nsv3911009copy number variation1nstd102humanPathogenic GRCh38 chr11: 119,424,297-135,075,271 , NCBI36 chr11: 118,800,217-134,450,377 , GRCh37 chr11: 119,295,007-134,945,165 DDX25, PHB1P17, 304 more genes
    nsv3922773copy number variation1nstd102humanPathogenic GRCh37 chr11: 119,304,619-134,868,407 , GRCh38 chr11: 119,433,909-134,998,513 , NCBI36 chr11: 118,809,829-134,373,617 DDX25, ETS1-AS1, 301 more genes
    nsv3906843copy number variation1nstd102humanPathogenic GRCh37 chr11: 119,538,664-134,938,470 , GRCh38.p12 chr11: 119,667,954-135,068,576 DDX25, TMEM225, 296 more genes
    nsv3902675copy number variation1nstd102humanPathogenic GRCh37 chr11: 119,807,473-134,868,407 , GRCh38.p12 chr11: 119,936,764-134,998,513 DDX25, FEZ1, 291 more genes
    nsv3923251copy number variation1nstd102humanPathogenic NCBI36 chr11: 119,891,678-134,450,377 , GRCh38 chr11: 120,515,759-135,075,271 , GRCh37 chr11: 120,386,468-134,945,165 DDX25, KIRREL3-AS3, 279 more genes
    nsv3901752copy number variation1nstd102humanPathogenic GRCh37 chr11: 120,527,021-134,938,470 , GRCh38.p12 chr11: 120,656,312-135,068,576 DDX25, LOC105369534, 276 more genes
    nsv4436748copy number variation1nstd102humanPathogenic GRCh37 chr11: 120,576,984-134,934,063 , GRCh38.p12 chr11: 120,706,275-135,064,169 DDX25, LINC02098, 276 more genes
    nsv3904760copy number variation1nstd102humanPathogenic GRCh37 chr11: 120,615,374-134,868,407 , GRCh38.p12 chr11: 120,744,665-134,998,513 DDX25, OR8D2, 275 more genes
    nsv4675832copy number variation1nstd102humanPathogenic GRCh37 chr11: 120,742,540-134,938,470 , GRCh38.p12 chr11: 120,871,831-135,068,576 DDX25, MIR8052, 275 more genes
    nsv3924566copy number variation1nstd102humanPathogenic GRCh38 chr11: 120,507,265-134,576,266 , NCBI36 chr11: 119,883,184-133,951,370 , GRCh37 chr11: 120,377,974-134,446,160 DDX25, CCDC15-DT, 271 more genes
    nsv3891701copy number variation1nstd102humanPathogenic GRCh37 chr11: 121,136,603-134,938,470 , GRCh38.p12 chr11: 121,265,894-135,068,576 DDX25, OR10G9, 266 more genes
    nsv7137129copy number variation1nstd102humanPathogenic GRCh37 chr11: 120,531,028-134,257,553 , GRCh38.p12 chr11: 120,660,319-134,387,659 DDX25, VSIG10L2, 268 more genes
    nsv3895234copy number variation1nstd102humanPathogenic GRCh37 chr11: 121,416,261-134,938,470 , GRCh38.p12 chr11: 121,545,552-135,068,576 DDX25, SF3A3P2, 262 more genes
    nsv3918400copy number variation1nstd102humanPathogenic GRCh37 chr11: 121,482,185-134,938,470 , GRCh38 chr11: 121,611,476-135,068,576 , NCBI36 chr11: 120,987,395-134,443,680 DDX25, RN7SL167P, 262 more genes
    nsv3915295copy number variation1nstd102humanPathogenic NCBI36 chr11: 121,064,970-134,450,377 , GRCh38 chr11: 121,689,052-135,075,271 , GRCh37 chr11: 121,559,760-134,945,165 DDX25, LOC105369591, 262 more genes
    nsv3892434copy number variation1nstd102humanPathogenic GRCh37 chr11: 121,501,072-134,868,348 , GRCh38.p12 chr11: 121,630,363-134,998,454 DDX25, ZNF123P, 261 more genes
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