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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4459353mobile element insertion1nstd166human GRCh37.p13 chr1: 169,760,819-169,760,819 , GRCh38.p12 chr1: 169,791,678-169,791,678 METTL18
    nsv7055606inversion1nstd229human GRCh38 chr1: 169,768,856-169,802,625 , GRCh37.p13 chr1: 169,737,997-169,771,766 METTL18, FIRRM
    nsv7052826inversion1nstd229human GRCh38 chr1: 169,783,637-169,805,219 , GRCh37.p13 chr1: 169,752,778-169,774,360 METTL18, FIRRM
    nsv5363987translocation1nstd200human GRCh38 chr1: 169,750,156-169,750,156 , GRCh38 chr1: 169,795,339-169,795,339 , GRCh37.p13 chr1: 169,764,480-169,764,480 , GRCh37.p13 chr1: 169,719,297-169,719,297 METTL18, FIRRM
    nsv5331296translocation1nstd200human GRCh37 chr1: 169,764,480-169,764,480 , GRCh37 chr1: 169,719,297-169,719,297 , GRCh38.p12 chr1: 169,750,156-169,750,156 , GRCh38.p12 chr1: 169,795,339-169,795,339 METTL18, FIRRM
    nsv4327615sequence alteration1nstd166human GRCh37.p13 chr1: 169,751,860-169,777,147 , GRCh38.p12 chr1: 169,782,719-169,808,006 METTL18, FIRRM
    nsv1503985short tandem repeat4nstd128human GRCh37 chr1: 169,763,047-169,763,062 , GRCh38.p12 chr1: 169,793,906-169,793,921 METTL18, FIRRM
    nsv6636331copy number variation1nstd102humanUncertain significance GRCh37 chr1: 169,723,387-169,775,456 , GRCh38.p12 chr1: 169,754,246-169,806,315 METTL18, LOC101928628, 1 more genes
    nsv4897971copy number variation1nstd200human GRCh38 chr1: 169,750,386-169,805,218 , GRCh37.p13 chr1: 169,719,527-169,774,359 METTL18, LOC101928628, 1 more genes
    nsv4784634copy number variation1nstd200human GRCh37 chr1: 169,719,527-169,774,359 , GRCh38.p12 chr1: 169,750,386-169,805,218 METTL18, FIRRM, 1 more genes
    nsv4061022copy number variation1nstd166human GRCh37.p13 chr1: 169,719,527-169,774,359 , GRCh38.p12 chr1: 169,750,386-169,805,218 METTL18, FIRRM, 1 more genes
    nsv7054060inversion1nstd229human GRCh38 chr1: 169,750,157-169,795,340 , GRCh37.p13 chr1: 169,719,298-169,764,481 METTL18, LOC101928628, 1 more genes
    nsv3912840copy number variation1nstd102humanPathogenic NCBI36 chr1: 144,764,751-247,199,719 , GRCh37.p13 chr1: 146,053,394-249,233,096 , GRCh38.p12 chr1: 120,836,007-206,268,643 METTL18, CRB1, 1608 more genes
    nsv3873192copy number variation1nstd102humanPathogenic GRCh37 chr1: 161,676,893-184,071,723 , GRCh38.p12 chr1: 161,707,103-184,102,589 METTL18, COLGALT2, 402 more genes
    nsv3889882copy number variation1nstd102humanPathogenic GRCh37 chr1: 159,815,642-177,026,983 , GRCh38.p12 chr1: 159,845,852-177,057,847 METTL18, FMO4, 403 more genes
    nsv4346684copy number variation1nstd102humanPathogenic GRCh37 chr1: 160,369,890-175,796,325 , GRCh38.p12 chr1: 160,400,100-175,827,189 METTL18, LINC00626, 359 more genes
    nsv3901593copy number variation1nstd102humanPathogenic NCBI36 chr1: 161,618,937-174,112,781 , GRCh37 chr1: 163,352,313-175,846,158 , GRCh38 chr1: 163,382,523-175,877,022 METTL18, NME7, 233 more genes
    nsv3894431copy number variation1nstd102humanPathogenic NCBI36 chr1: 159,977,321-172,200,915 , GRCh37 chr1: 161,710,697-173,934,292 , GRCh38 chr1: 161,740,907-173,965,154 METTL18, RPL21P27, 238 more genes
    nsv6313719copy number variation1nstd102humanPathogenic GRCh37 chr1: 162,330,810-171,532,331 , GRCh38.p12 chr1: 162,361,020-171,563,192 METTL18, LOC100420658, 167 more genes
    nsv3896314copy number variation1nstd102humanPathogenic GRCh37 chr1: 169,187,474-178,044,969 , NCBI36 chr1: 167,454,098-176,311,592 , GRCh38 chr1: 169,218,236-178,075,834 METTL18, RPS26P12, 150 more genes
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