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Items: 1 to 20 of 192

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5946150copy number variation1nstd209human GRCh38 chr19: 45,309,513-45,309,819 , GRCh37.p13 chr19: 45,812,771-45,813,077 CKM
    nsv5934182copy number variation1nstd209human GRCh38 chr19: 45,310,891-45,311,353 , GRCh37.p13 chr19: 45,814,149-45,814,611 CKM
    nsv5591359copy number variation1nstd207human GRCh38 chr19: 45,310,891-45,311,353 , GRCh37.p13 chr19: 45,814,149-45,814,611 CKM
    nsv5529422copy number variation1nstd206human GRCh38 chr19: 45,310,743-45,311,092 , GRCh37.p13 chr19: 45,814,001-45,814,350 CKM
    nsv5523862copy number variation1nstd206human GRCh38 chr19: 45,310,891-45,311,354 , GRCh37.p13 chr19: 45,814,149-45,814,612 CKM
    nsv5518746copy number variation1nstd206human GRCh38 chr19: 45,233,921-45,349,653 , GRCh37.p13 chr19: 45,737,179-45,852,911 CKM, ERCC2, 5 more genes
    nsv5518080copy number variation1nstd206human GRCh38 chr19: 45,310,322-45,310,982 , GRCh37.p13 chr19: 45,813,580-45,814,240 CKM
    nsv5201467mobile element deletion1nstd204human GRCh38.p13 chr19: 45,310,091-45,310,446 , GRCh37.p13 chr19: 45,813,349-45,813,704 CKM
    nsv5024722copy number variation1nstd200human GRCh38 chr19: 45,264,836-45,399,221 , GRCh37.p13 chr19: 45,768,094-45,902,479 CKM, PPP1R13L, 4 more genes
    nsv5024720copy number variation1nstd200human GRCh38 chr19: 45,233,941-45,349,633 , GRCh37.p13 chr19: 45,737,199-45,852,891 KLC3, CKM, 5 more genes
    nsv5020681copy number variation1nstd200human GRCh38 chr19: 45,308,986-45,312,590 , GRCh37.p13 chr19: 45,812,244-45,815,848 CKM
    nsv4907550mobile element deletion1nstd200human GRCh38 chr19: 45,310,772-45,311,070 , GRCh37.p13 chr19: 45,814,030-45,814,328 CKM
    nsv4853069copy number variation1nstd200human GRCh37 chr19: 45,812,251-45,812,534 , GRCh38.p12 chr19: 45,308,993-45,309,276 CKM
    nsv4775426mobile element deletion1nstd200human GRCh37 chr19: 45,817,972-45,818,241 , GRCh38.p12 chr19: 45,314,714-45,314,983 CKM
    nsv4775425mobile element deletion1nstd200human GRCh37 chr19: 45,814,030-45,814,328 , GRCh38.p12 chr19: 45,310,772-45,311,070 CKM
    nsv4775424mobile element deletion1nstd200human GRCh37 chr19: 45,813,378-45,813,676 , GRCh38.p12 chr19: 45,310,120-45,310,418 CKM
    nsv4701966copy number variation1nstd195human GRCh37 chr19: 45,814,149-45,814,150 , GRCh38.p12 chr19: 45,310,891-45,310,892 CKM
    nsv4676357copy number variation1nstd102humanPathogenic GRCh37 chr19: 44,738,088-53,621,561 , GRCh38.p12 chr19: 44,233,935-53,118,308 MIR4324, KLK9, 485 more genes
    nsv4676350copy number variation1nstd102humanUncertain significance GRCh37 chr19: 45,531,056-48,174,177 , GRCh38.p12 chr19: 45,027,798-47,670,920 NKPD1, IGFL1, 112 more genes
    nsv4676133copy number variation1nstd102humanUncertain significance GRCh37 chr19: 45,765,313-45,968,157 , GRCh38.p12 chr19: 45,262,055-45,464,899 MARK4, KLC3, 7 more genes
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