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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3877319copy number variation1nstd102humanBenign GRCh37 chr1: 77,768,016-77,781,567 , GRCh38.p12 chr1: 77,302,331-77,315,882 AK5
    nsv3906156copy number variation1nstd102humanLikely benign NCBI36 chr1: 77,502,835-77,731,275 , GRCh38 chr1: 77,264,562-77,493,002 , GRCh37 chr1: 77,730,247-77,958,687 AK5, RNU7-8P
    nsv3884822copy number variation1nstd102humanBenign GRCh37 chr1: 77,955,577-78,040,287 , GRCh38.p12 chr1: 77,489,892-77,574,602 AK5, ZZZ3
    nsv3905378copy number variation1nstd102humanUncertain significance NCBI36 chr1: 77,495,266-77,748,487 , GRCh37 chr1: 77,722,678-77,975,899 , GRCh38 chr1: 77,256,993-77,510,214 AK5, RNU7-8P
    nsv3881556copy number variation1nstd102humanUncertain significance GRCh37 chr1: 77,717,646-77,970,795 , GRCh38.p12 chr1: 77,251,961-77,505,110 RNU7-8P, AK5
    nsv3875209copy number variation1nstd102humanUncertain significance GRCh37 chr1: 77,722,678-77,970,795 , GRCh38.p12 chr1: 77,256,993-77,505,110 AK5, RNU7-8P
    nsv6313507copy number variation1nstd102humanUncertain significance GRCh37 chr9: 4,686,222-4,758,044 , GRCh38.p12 chr9: 4,686,222-4,758,044 CDC37L1, AK3
    nsv4453217copy number variation1nstd102humanUncertain significance GRCh37 chr1: 77,954,138-78,053,851 , GRCh38.p12 chr1: 77,488,453-77,588,166 ZZZ3, AK5
    nsv4675414copy number variation1nstd102humanLikely benign GRCh37 chr9: 4,733,991-4,809,077 , GRCh38.p12 chr9: 4,733,991-4,809,077 AK3, KLF4P1, 3 more genes
    nsv3889848copy number variation1nstd102humanPathogenic GRCh37 chr5: 17,628,741-176,575,720 , GRCh38.p12 chr5: 17,628,632-177,148,719 AK6, MEGF10, 2080 more genes
    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 ROR1, RNA5SP51, 333 more genes
    nsv6313574copy number variation1nstd102humanPathogenic GRCh37 chr1: 68,180,293-92,731,957 , GRCh38.p12 chr1: 67,714,610-92,266,400 RNA5SP51, ADGRL4, 315 more genes
    nsv3886551copy number variation1nstd102humanPathogenic GRCh37 chr1: 64,321,264-88,153,669 , GRCh38.p12 chr1: 63,855,593-87,687,986 RNU6-1102P, RAVER2, 291 more genes
    nsv3885743copy number variation1nstd102humanPathogenic GRCh37 chr1: 72,044,544-92,505,091 , GRCh38.p12 chr1: 71,578,861-92,039,534 ZNHIT6, CCN1, 257 more genes
    nsv3920950copy number variation1nstd102humanPathogenic NCBI36 chr9: 194,104-18,872,279 , GRCh37 chr9: 204,104-18,882,279 , GRCh38 chr9: 204,104-18,882,281 RPL4P5, SMARCA2, 193 more genes
    nsv3910019copy number variation1nstd102humanPathogenic GRCh38 chr9: 220,253-18,708,805 , NCBI36 chr9: 210,253-18,698,803 , GRCh37 chr9: 220,253-18,708,803 LOC107987049, RNU2-47P, 191 more genes
    nsv5381767copy number variation1nstd102humanPathogenic GRCh37 chr9: 204,193-18,654,812 , GRCh38.p12 chr9: 204,193-18,654,814 ACTG1P14, DMAC1, 191 more genes
    nsv4454000copy number variation1nstd102humanPathogenic GRCh37 chr1: 67,851,233-86,101,340 , GRCh38.p12 chr1: 67,385,550-85,635,657 NEXN, LOC107985391, 209 more genes
    nsv3884583copy number variation1nstd102humanPathogenic GRCh37 chr1: 61,351,024-79,583,933 , GRCh38.p12 chr1: 60,885,352-79,118,248 MIR7156, CHORDC1P5, 243 more genes
    nsv4768366copy number variation1nstd102humanPathogenic GRCh37 chr9: 204,193-18,073,357 , GRCh38.p12 chr9: 204,193-18,073,359 DOCK8-AS1, RN7SL25P, 186 more genes
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