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Items: 1 to 20 of 309

  • The following terms were not found in dbVar: Bromo, picoline.
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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6314411complex chromosomal rearrangement2nstd102humanLikely pathogenic GRCh38.p12 chr4: 110,832,775-110,832,775 , GRCh38.p12 chr4: 110,832,999-110,832,999 , GRCh37 chr4: 111,753,931-111,753,931 , GRCh37 chr4: 111,754,155-111,754,155 , GRCh38.p12 chr2: 44,373,713-44,373,713 , GRCh38.p12 chr2: 44,374,328-44,374,328 , GRCh37 chr2: 44,600,852-44,600,852 , GRCh37 chr2: 44,601,467-44,601,467 CAMKMT
    nsv6686785copy number variation1nstd229human GRCh38 chr2: 89,671,963-89,675,830 , GRCh37.p13 chr4: 103,860,695-103,864,591 IGK
    nsv5438285copy number variation1nstd206human GRCh38 chr2: 89,671,943-89,675,850 , GRCh37.p13 chr4: 103,860,675-103,864,611 IGK
    nsv5990599copy number variation1nstd212human GRCh38 chr2: 89,671,960-89,675,830 , GRCh37.p13 chr4: 103,860,695-103,864,594 IGK
    nsv5569471copy number variation1nstd207human GRCh38 chr2: 89,671,960-89,675,829 , GRCh37.p13 chr4: 103,860,696-103,864,594 IGK
    nsv5289055copy number variation1nstd204human GRCh38.p13 chr2: 89,671,962-89,675,830 , GRCh37.p13 chr4: 103,860,694-103,864,591 IGK
    nsv5873106copy number variation1nstd209human GRCh38 chr2: 89,671,960-89,675,829 , GRCh37.p13 chr4: 103,860,696-103,864,594 IGK
    nsv4907948copy number variation1nstd200human GRCh38 chr2: 89,671,963-89,675,830 , GRCh37.p13 chr4: 103,860,695-103,864,591 IGK
    nsv3524850copy number variation4nstd152human GRCh38 chr2: 89,671,960-89,675,831 , GRCh37.p13 chr4: 103,860,695-103,864,595 IGK
    nsv3234533mobile element deletion1nstd152human GRCh38 chr2: 89,671,967-89,675,836 , GRCh37.p13 chr4: 103,860,689-103,864,587 IGK
    nsv3367411copy number variation1nstd162human GRCh38 chr2: 89,671,962-89,675,831 , GRCh37.p13 chr4: 103,860,694-103,864,592 IGK
    nsv937111copy number variation1nstd84human GRCh37 chr2: 96,546,177-96,604,650 , GRCh38.p12 chr2: 95,880,429-95,938,902 ANKRD36C
    nsv935518copy number variation1nstd84human GRCh37 chr2: 89,082,253-89,104,923 , GRCh38.p12 chr2: 88,782,736-88,805,409 ANKRD36BP2
    nsv935868copy number variation1nstd84human GRCh37 chr2: 97,684,094-97,703,287 , GRCh38.p12 chr2: 97,018,357-97,037,550 TRIM43CP
    nsv936597copy number variation1nstd84human GRCh37 chr4: 18,671,410-18,688,946 , GRCh38.p12 chr4: 18,669,787-18,687,323 LOC105374510
    nsv935227copy number variation1nstd84human GRCh37 chr2: 1,525,546-1,541,155 , GRCh38.p12 chr2|NT_187529.1: 204,145-219,754 , GRCh38.p12 chr2: 1,521,774-1,537,383 TPO
    nsv936211copy number variation1nstd84human GRCh37 chr4: 187,881,413-187,894,167 , GRCh38.p12 chr4: 186,960,259-186,973,013 LOC102723906
    nsv936031copy number variation1nstd84human GRCh37 chr2: 131,317,751-131,327,574 , GRCh38.p12 chr2: 130,560,178-130,570,001 PRSS40A
    nsv936263copy number variation1nstd84human GRCh37 chr4: 172,987,844-172,995,932 , GRCh38.p12 chr4: 172,066,693-172,074,781 GALNTL6
    nsv934345copy number variation1nstd84human GRCh37 chr2: 86,559,057-86,566,470 , GRCh38.p12 chr2: 86,331,934-86,339,347 REEP1
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