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Items: 1 to 20 of 308623

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

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3879671copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr4: 55,524,176-55,604,729 , GRCh38.p12 chr4: 54,658,009-54,738,563 KIT
    nsv3879923copy number variation1nstd102humanPathogenic GRCh37 chr4: 88,928,866-88,996,866 , GRCh38 chr4: 88,007,714-88,075,714 PKD2
    nsv3888170copy number variation1nstd102humanPathogenic GRCh38 chr4: 88,007,714-88,058,123 , GRCh37 chr4: 88,928,866-88,979,275 PKD2
    nsv3883954copy number variation1nstd102humanPathogenic GRCh38 chr4: 92,559,959-92,610,106 , GRCh37 chr4: 93,481,112-93,531,259 GRID2
    nsv4683511copy number variation1nstd102humanPathogenic GRCh37 chr4: 88,959,383-88,996,866 , GRCh38.p12 chr4: 88,038,231-88,075,714 PKD2
    nsv3878603copy number variation1nstd102humanPathogenic GRCh38 chr4: 93,098,691-93,135,614 , GRCh37 chr4: 94,019,842-94,056,765 GRID2
    nsv3875642copy number variation1nstd102humanPathogenic GRCh38 chr4: 154,580,323-154,590,216 , GRCh37.p13 chr4: 155,501,475-155,511,368 FGA
    nsv4716560copy number variation1nstd102humanPathogenic GRCh38 chr4: 154,740,841-154,749,136 , GRCh37.p13 chr4: 155,661,993-155,670,288 LRAT
    nsv6314976copy number variation1nstd102humanPathogenic GRCh37 chr4: 512,202-518,547 , GRCh38 chr4: 518,413-524,758 PIGG
    nsv6314984copy number variation1nstd102humanPathogenic GRCh37 chr4: 493,968-499,930 , GRCh38 chr4: 500,179-506,141 PIGG
    nsv7097257copy number variation1nstd102humanPathogenic GRCh37 chr4: 55,569,880-55,570,068 , GRCh38.p12 chr4: 54,703,714-54,703,902 KIT
    nsv6634501copy number variation1nstd102humanPathogenic GRCh37 chr4: 25,657,344-25,657,529 , GRCh38 chr4: 25,655,722-25,655,907 SLC34A2
    nsv6311728copy number variation1nstd102humanPathogenic GRCh37 chr4: 56,225,493-56,225,675 , GRCh38.p12 chr4: 55,359,326-55,359,508 SRD5A3
    nsv4685719copy number variation1nstd102humanPathogenic GRCh37 chr4: 107,092,252-107,092,428 , GRCh38.p12 chr4: 106,171,095-106,171,271 TBCK
    nsv997226copy number variation1nstd45humanPathogenic GRCh38.p12 chr4: 88,007,647-88,077,779 , GRCh37 chr4: 88,928,799-88,998,931 PKD2
    nsv997231copy number variation1nstd45humanPathogenic GRCh38.p12 chr4: 110,617,423-110,642,123 , GRCh37 chr4: 111,538,579-111,563,279 PITX2
    nsv4684109copy number variation1nstd102humanPathogenic GRCh37 chr4: 619,583-619,584 , GRCh38 chr4: 625,794-625,795 PDE6B
    nsv7098697insertion3nstd102humanPathogenic GRCh38 chr4: 41,745,972-41,746,045 , GRCh37.p13 chr4: 41,747,989-41,748,062 PHOX2B
    nsv6314972delins1nstd102humanPathogenic GRCh37 chr4: 499,456-499,529 , GRCh38 chr4: 505,667-505,740 PIGG
    nsv4352980delins3nstd102humanPathogenic GRCh37 chr4: 39,350,045-39,350,099 , GRCh38.p12 chr4: 39,348,425-39,348,479 RFC1
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    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
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