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Items: 1 to 20 of 109

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4683964copy number variation1nstd102humanPathogenic GRCh37 chr5: 7,878,047-7,878,445 , GRCh38.p12 chr5: 7,877,934-7,878,332 MTRR
    nsv7097292copy number variation1nstd102humanPathogenic GRCh37 chr5: 7,870,908-7,871,056 , GRCh38.p12 chr5: 7,870,795-7,870,943 MTRR
    nsv7097545copy number variation1nstd102humanPathogenic GRCh37 chr5: 7,875,361-7,875,498 , GRCh38.p12 chr5: 7,875,248-7,875,385 MTRR
    nsv6312117copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr5: 7,870,908-7,900,171 , GRCh38.p12 chr5: 7,870,795-7,900,058 MTRR
    nsv4683570copy number variation1nstd102humanLikely pathogenic GRCh37 chr5: 7,883,258-7,893,036 , GRCh38.p12 chr5: 7,883,145-7,892,923 MTRR
    nsv6312007copy number variation1nstd102humanLikely pathogenic GRCh37 chr5: 7,889,198-7,897,370 , GRCh38.p12 chr5: 7,889,085-7,897,257 MTRR
    nsv4685628copy number variation1nstd102humanLikely pathogenic GRCh37 chr5: 7,885,880-7,887,275 , GRCh38 chr5: 7,885,767-7,887,162 MTRR
    nsv6312211copy number variation1nstd102humanUncertain significance GRCh37 chr5: 7,895,827-7,900,171 , GRCh38.p12 chr5: 7,895,714-7,900,058 MTRR
    nsv4682276copy number variation1nstd102humanPathogenic GRCh37 chr5: 7,869,227-7,900,191 , GRCh38.p12 chr5: 7,869,114-7,900,078 MTRR, FASTKD3
    nsv3914649copy number variation1nstd102humanPathogenic GRCh38 chr5: 22,149-35,831,538 , GRCh37 chr5: 22,149-35,831,640 , NCBI36 chr5: 75,149-35,867,397 MTRR, LOC105374666, 399 more genes
    nsv3887142copy number variation1nstd102humanPathogenic GRCh37 chr5: 22,149-34,041,196 , GRCh38.p12 chr5: 22,149-34,041,091 MTRR, H3Y1, 381 more genes
    nsv3910712copy number variation1nstd102humanPathogenic NCBI36 chr5: 166,576-34,034,151 , GRCh38 chr5: 113,461-33,998,289 , GRCh37 chr5: 113,576-33,998,394 MTRR, ROPN1L, 378 more genes
    nsv3924496copy number variation1nstd102humanPathogenic GRCh37 chr5: 22,149-32,248,116 , NCBI36 chr5: 75,149-32,283,873 , GRCh38 chr5: 22,149-32,248,010 MTRR, LOC105374678, 356 more genes
    nsv6636942copy number variation1nstd102humanPathogenic GRCh37 chr5: 1-32,091,038 , GRCh38.p12 chr5: 10,001-32,090,932 MTRR, LOC105374608, 351 more genes
    nsv6636606copy number variation1nstd102humanPathogenic GRCh37 chr5: 113,577-31,448,527 , GRCh38.p12 chr5: 113,462-31,448,420 MTRR, BASP1, 338 more genes
    nsv3881706copy number variation1nstd102humanPathogenic GRCh37 chr5: 25,328-31,343,671 , GRCh38.p12 chr5: 25,329-31,343,564 MTRR, IRX2-DT, 339 more genes
    nsv3883796copy number variation1nstd102humanPathogenic GRCh37 chr5: 25,328-30,672,798 , GRCh38.p12 chr5: 25,329-30,672,691 MTRR, H3P22, 335 more genes
    nsv6315416copy number variation1nstd102humanPathogenic GRCh37 chr5: 113,576-30,712,376 , GRCh38.p12 chr5: 113,461-30,712,269 MTRR, LOC105374649, 333 more genes
    nsv3912696copy number variation1nstd102humanPathogenic GRCh37 chr5: 50,093-30,112,642 , GRCh38 chr5: 49,978-30,112,535 , NCBI36 chr5: 103,093-30,148,399 MTRR, OTULINL, 333 more genes
    nsv5381771copy number variation1nstd102humanPathogenic GRCh37 chr5: 22,149-29,048,823 , GRCh38.p12 chr5: 22,149-29,048,716 MTRR, OTULINL, 317 more genes
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