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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3888386copy number variation1nstd102humanPathogenic GRCh38 chr2: 50,721,552-50,944,617 , GRCh37.p13 chr2: 50,948,690-51,171,755 NRXN1
    nsv3883664copy number variation1nstd102humanPathogenic GRCh38 chr2: 148,139,385-148,242,336 , GRCh37.p13 chr2: 148,896,954-148,999,905 MBD5
    nsv3880996copy number variation1nstd102humanPathogenic GRCh38 chr2: 148,157,591-148,226,058 , GRCh37.p13 chr2: 148,915,160-148,983,627 MBD5
    nsv3873116copy number variation1nstd102humanPathogenic GRCh38 chr2: 148,158,424-148,226,279 , GRCh37.p13 chr2: 148,915,993-148,983,848 MBD5
    nsv3872646copy number variation1nstd102humanLikely pathogenic GRCh38 chr2: 205,264,941-205,497,509 , GRCh37.p13 chr2: 206,129,665-206,362,233 PARD3B
    nsv3872214copy number variation1nstd102humanLikely pathogenic GRCh38 chr16: 6,360,351-6,582,207 , GRCh37.p13 chr16: 6,410,352-6,632,208 RBFOX1
    nsv3884102copy number variation1nstd102humanLikely pathogenic GRCh38 chr10: 54,690,788-54,898,513 , GRCh37.p13 chr10: 56,450,548-56,658,273 PCDH15
    nsv3878136copy number variation1nstd102humanLikely pathogenic GRCh38 chr6: 161,816,395-162,018,868 , GRCh37.p13 chr6: 162,237,427-162,439,900 PRKN
    nsv3871099copy number variation1nstd102humanLikely pathogenic GRCh38 chr3: 60,389,119-60,571,624 , GRCh37.p13 chr3: 60,374,852-60,557,357 FHIT
    nsv3870976copy number variation1nstd102humanLikely pathogenic GRCh38 chr8: 99,047,163-99,227,439 , GRCh37.p13 chr8: 100,059,391-100,239,667 VPS13B
    nsv3884820copy number variation1nstd102humanLikely pathogenic GRCh38 chr11: 84,809,995-84,986,152 , GRCh37.p13 chr11: 84,521,038-84,697,196 DLG2
    nsv3872572copy number variation1nstd102humanLikely pathogenic GRCh38 chr4: 92,930,845-93,092,974 , GRCh37.p13 chr4: 93,851,996-94,014,125 GRID2
    nsv3879657copy number variation1nstd102humanLikely pathogenic GRCh38 chr6: 161,933,685-162,059,574 , GRCh37.p13 chr6: 162,354,717-162,480,606 PRKN
    nsv3870510copy number variation1nstd102humanLikely pathogenic GRCh38 chr3: 188,420,063-188,540,464 , GRCh37.p13 chr3: 188,137,851-188,258,252 LPP
    nsv3873197copy number variation1nstd102humanLikely pathogenic GRCh38 chr16: 6,622,570-6,720,408 , GRCh37.p13 chr16: 6,672,571-6,770,409 RBFOX1
    nsv3872051copy number variation1nstd102humanLikely pathogenic GRCh38 chr2: 205,102,232-205,198,713 , GRCh37.p13 chr2: 205,966,956-206,063,437 PARD3B
    nsv3878782copy number variation1nstd102humanLikely pathogenic GRCh38 chr3: 188,343,948-188,435,451 , GRCh37.p13 chr3: 188,061,736-188,153,239 LPP
    nsv3872038copy number variation1nstd102humanLikely pathogenic GRCh38 chr8: 3,876,145-3,967,152 , GRCh37.p13 chr8: 3,733,667-3,824,674 CSMD1
    nsv3879838copy number variation1nstd102humanLikely pathogenic GRCh38 chr20: 42,472,130-42,562,200 , GRCh37.p13 chr20: 41,100,770-41,190,840 PTPRT
    nsv3881398copy number variation1nstd102humanLikely pathogenic GRCh38 chr8: 3,873,130-3,959,547 , GRCh37.p13 chr8: 3,730,652-3,817,069 CSMD1
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