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Items: 1 to 20 of 87

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3901546copy number variation1nstd102humanPathogenic NCBI36 chr1: 59,057,865-86,336,882 , GRCh37 chr1: 59,285,277-86,564,294 , GRCh38 chr1: 58,819,605-86,098,611 CTH, ROR1, 333 more genes
    nsv6313574copy number variation1nstd102humanPathogenic GRCh37 chr1: 68,180,293-92,731,957 , GRCh38.p12 chr1: 67,714,610-92,266,400 CTH, RNA5SP51, 315 more genes
    nsv3886551copy number variation1nstd102humanPathogenic GRCh37 chr1: 64,321,264-88,153,669 , GRCh38.p12 chr1: 63,855,593-87,687,986 CTH, RNU6-1102P, 291 more genes
    nsv4454000copy number variation1nstd102humanPathogenic GRCh37 chr1: 67,851,233-86,101,340 , GRCh38.p12 chr1: 67,385,550-85,635,657 CTH, NEXN, 209 more genes
    nsv3884583copy number variation1nstd102humanPathogenic GRCh37 chr1: 61,351,024-79,583,933 , GRCh38.p12 chr1: 60,885,352-79,118,248 CTH, MIR7156, 243 more genes
    nsv3903468copy number variation1nstd102humanPathogenic NCBI36 chr1: 59,870,760-76,969,150 , GRCh37 chr1: 60,098,172-77,196,562 , GRCh38 chr1: 59,632,500-76,730,877 CTH, WLS, 219 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 PHB1P17, KIRREL3, 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 ETS1-AS1, SLC37A2, 301 more genes
    nsv3906843copy number variation1nstd102humanPathogenic GRCh37 chr11: 119,538,664-134,938,470 , GRCh38.p12 chr11: 119,667,954-135,068,576 TMEM225, OR6M2P, 296 more genes
    nsv3902675copy number variation1nstd102humanPathogenic GRCh37 chr11: 119,807,473-134,868,407 , GRCh38.p12 chr11: 119,936,764-134,998,513 FEZ1, OR6M1, 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 KIRREL3-AS3, OR8B4, 279 more genes
    nsv3901752copy number variation1nstd102humanPathogenic GRCh37 chr11: 120,527,021-134,938,470 , GRCh38.p12 chr11: 120,656,312-135,068,576 LOC105369534, SORL1, 276 more genes
    nsv4436748copy number variation1nstd102humanPathogenic GRCh37 chr11: 120,576,984-134,934,063 , GRCh38.p12 chr11: 120,706,275-135,064,169 LINC02098, LOC105369587, 276 more genes
    nsv3904760copy number variation1nstd102humanPathogenic GRCh37 chr11: 120,615,374-134,868,407 , GRCh38.p12 chr11: 120,744,665-134,998,513 OR8D2, PHB1P17, 275 more genes
    nsv4675832copy number variation1nstd102humanPathogenic GRCh37 chr11: 120,742,540-134,938,470 , GRCh38.p12 chr11: 120,871,831-135,068,576 MIR8052, BLID, 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 CCDC15-DT, LOC105369544, 271 more genes
    nsv3909388copy number variation1nstd102humanPathogenic GRCh37 chr1: 57,816,246-71,791,607 , GRCh38 chr1: 57,350,574-71,325,924 , NCBI36 chr1: 57,588,834-71,564,195 CTH, RNU6-1031P, 193 more genes
    nsv3891701copy number variation1nstd102humanPathogenic GRCh37 chr11: 121,136,603-134,938,470 , GRCh38.p12 chr11: 121,265,894-135,068,576 OR10G9, LINC02706, 266 more genes
    nsv7137129copy number variation1nstd102humanPathogenic GRCh37 chr11: 120,531,028-134,257,553 , GRCh38.p12 chr11: 120,660,319-134,387,659 VSIG10L2, OR8B6P, 268 more genes
    nsv3895234copy number variation1nstd102humanPathogenic GRCh37 chr11: 121,416,261-134,938,470 , GRCh38.p12 chr11: 121,545,552-135,068,576 SF3A3P2, RN7SKP279, 262 more genes
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