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Items: 1 to 20 of 32

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5980420copy number variation1nstd102humanLikely benign GRCh37 chr19: 49,661,114-49,675,375 , GRCh38.p12 chr19: 49,157,857-49,172,118 TRPM4
    nsv6310697copy number variation1nstd102humanUncertain significance GRCh37 chr19: 49,661,124-49,669,492 , GRCh38.p12 chr19: 49,157,867-49,166,235 TRPM4
    nsv4683180copy number variation1nstd102humanUncertain significance GRCh37 chr19: 49,661,114-49,669,482 , GRCh38.p12 chr19: 49,157,857-49,166,225 TRPM4
    nsv3878583copy number variation1nstd102humanUncertain significance GRCh38 chr19: 49,166,021-49,172,128 , GRCh37 chr19: 49,669,278-49,675,385 TRPM4
    nsv4681254copy number variation1nstd102humanUncertain significance GRCh37 chr19: 49,669,288-49,675,375 , GRCh38.p12 chr19: 49,166,031-49,172,118 TRPM4
    nsv6310698copy number variation2nstd102humanUncertain significance GRCh37 chr19: 49,713,446-49,714,755 , GRCh38.p12 chr19: 49,210,189-49,211,498 TRPM4
    nsv7095661copy number variation1nstd102humanUncertain significance GRCh37 chr19: 49,705,201-49,705,418 , GRCh38.p12 chr19: 49,201,944-49,202,161 TRPM4
    nsv5381198copy number variation1nstd102humanUncertain significance GRCh37 chr19: 49,705,211-49,705,408 , GRCh38.p12 chr19: 49,201,954-49,202,151 TRPM4
    nsv4682759copy number variation1nstd102humanUncertain significance GRCh37 chr19: 49,684,596-49,684,728 , GRCh38.p12 chr19: 49,181,339-49,181,471 TRPM4
    nsv3882779copy number variation1nstd102humanUncertain significance GRCh38 chr19: 49,157,847-49,172,128 , GRCh37.p13 chr19: 49,661,104-49,675,385 TRPM4
    nsv7095660copy number variation1nstd102humanUncertain significance GRCh37 chr19: 49,684,586-49,694,050 , GRCh38.p12 chr19: 49,181,329-49,190,793 TRPM4
    nsv5564402copy number variation1nstd102humanUncertain significance GRCh37 chr19: 49,684,596-49,694,040 , GRCh38.p12 chr19: 49,181,339-49,190,783 TRPM4
    nsv6310642copy number variation1nstd102humanUncertain significance GRCh37 chr19: 49,684,586-49,686,489 , GRCh38.p12 chr19: 49,181,329-49,183,232 TRPM4
    nsv3906791copy number variation1nstd102humanBenign GRCh37 chr19: 49,651,042-49,660,889 , GRCh38.p12 chr19: 49,147,785-49,157,632 TRPM4, HRC, 1 more genes
    nsv3894112copy number variation1nstd102humanLikely benign GRCh37 chr19: 49,640,430-49,703,840 , GRCh38.p12 chr19: 49,137,173-49,200,583 TRPM4, HRC, 1 more genes
    nsv3891859copy number variation1nstd102humanBenign GRCh37 chr19: 49,635,951-49,678,085 , GRCh38.p12 chr19: 49,132,694-49,174,828 TRPM4, HRC, 1 more genes
    nsv3903230copy number variation1nstd102humanBenign GRCh37 chr19: 49,635,951-49,675,233 , GRCh38.p12 chr19: 49,132,694-49,171,976 TRPM4, PPFIA3, 1 more genes
    nsv3901004copy number variation1nstd102humanBenign GRCh37 chr19: 49,640,002-49,675,233 , GRCh38.p12 chr19: 49,136,745-49,171,976 TRPM4, HRC, 1 more genes
    nsv4685766copy number variation1nstd102humannot provided GRCh37 chr19: 49,640,430-49,703,884 , GRCh38.p12 chr19: 49,137,173-49,200,627 TRPM4, HRC, 1 more genes
    nsv6315030copy number variation1nstd102humanUncertain significance GRCh38 chr19: 49,131,439-49,174,442 , GRCh37.p13 chr19: 49,634,696-49,677,699 TRPM4, PPFIA3, 1 more genes
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