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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6130884insertion1nstd186human GRCh37 chr21: 10,697,897-44,966,043 , GRCh38.p12 chr21: 12,965,809-43,546,162 , APP, 533 more genes
    nsv5564322copy number variation2nstd102humanUncertain significance GRCh37 chr21: 44,838,130-45,196,150 , GRCh38.p12 chr21: 43,418,250-43,776,269 LINC00319, HSF2BP, 10 more genes
    nsv5287156copy number variation1nstd204human GRCh38.p13 chr21: 43,034,901-43,571,900 , GRCh37.p13 chr21: 44,455,011-44,991,781 , HSF2BP, 18 more genes
    nsv4730021copy number variation1nstd102humanPathogenic GRCh37 chr21: 14,629,063-48,090,317 , GRCh38.p12 chr21: 13,256,742-46,670,405 SLX9, LOC105372750, 619 more genes
    nsv4729811copy number variation1nstd102humanUncertain significance GRCh37 chr21: 44,717,197-44,926,001 , GRCh38.p12 chr21: 43,297,317-43,506,121 LOC102723380, LINC00313, 6 more genes
    nsv4682475copy number variation1nstd102humanPathogenic GRCh37 chr21: 44,836,602-45,629,566 , GRCh38.p12 chr21: 43,416,722-44,209,683 LINC00313, LOC105372826, 27 more genes
    nsv4682183copy number variation3nstd102humanUncertain significance, Pathogenic GRCh37 chr21: 44,838,120-45,629,566 , GRCh38.p12 chr21: 43,418,240-44,209,683 RRP1, LINC00313, 27 more genes
    nsv4681891copy number variation1nstd102humanUncertain significance GRCh37 chr21: 43,792,871-46,330,697 , GRCh38.p12 chr21: 42,372,762-44,910,782 DNMT3L-AS1, WDR4, 100 more genes
    nsv4679058copy number variation1nstd189human GRCh37.p13 chr21: 14,468,835-48,129,895 , GRCh38.p12 chr21: 13,096,514-46,699,983 , ADARB1, 652 more genes
    nsv4676376copy number variation1nstd102humanPathogenic GRCh37 chr21: 43,472,147-48,097,372 , GRCh38.p12 chr21: 42,052,038-46,677,460 LOC101928369, MTND6P21, 157 more genes
    nsv4676372copy number variation1nstd102humanPathogenic GRCh37 chr21: 39,410,438-45,171,756 , GRCh38.p12 chr21: 38,038,136-43,751,875 KCNJ15, SPATA20P1, 126 more genes
    nsv4676330copy number variation1nstd102humanLikely benign GRCh37 chr21: 44,620,109-44,958,565 , GRCh38.p12 chr21: 43,199,999-43,538,685 HSF2BP, LINC00319, 6 more genes
    nsv4676321copy number variation1nstd102humanPathogenic GRCh37 chr21: 42,044,877-48,100,155 , GRCh38.p12 chr21: 40,672,951-46,680,243 SLC19A1, LINC03039, 183 more genes
    nsv4676320copy number variation1nstd102humanUncertain significance GRCh37 chr21: 44,736,485-44,968,648 , GRCh38.p12 chr21: 43,316,605-43,548,767 HSF2BP, LINC01679, 6 more genes
    nsv4676282copy number variation1nstd102humanLikely benign GRCh37 chr21: 44,847,202-45,265,689 , GRCh38.p12 chr21: 43,427,322-43,845,808 MIR6070, TMEM97P1, 14 more genes
    nsv4676186copy number variation1nstd102humanUncertain significance GRCh37 chr21: 43,822,539-44,974,001 , GRCh38.p12 chr21: 42,402,430-43,554,120 UBASH3A, HSF2BP, 34 more genes
    nsv4457830copy number variation1nstd102humanPathogenic GRCh37 chr21: 43,756,585-46,240,105 , GRCh38.p12 chr21: 42,336,476-44,820,190 RSPH1-DT, PKNOX1, 100 more genes
    nsv4457803copy number variation1nstd102humanPathogenic GRCh37 chr21: 44,310,057-47,503,155 , GRCh38.p12 chr21: 42,889,947-46,083,241 SLX9, PICSAR, 114 more genes
    nsv4457558copy number variation1nstd102humanUncertain significance GRCh37 chr21: 44,577,746-45,120,173 , GRCh38.p12 chr21: 43,157,636-43,700,292 LINC01679, LOC107987300, 13 more genes
    nsv4457505copy number variation1nstd102humanUncertain significance GRCh37 chr21: 44,735,958-45,448,138 , GRCh38.p12 chr21: 43,316,078-44,028,257 RNU6-1150P, CSTB, 24 more genes
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