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Items: 1 to 20 of 167

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3901746copy number variation1nstd102humanBenign GRCh37 chr14: 35,992,878-36,004,713 , GRCh38.p12 chr14: 35,523,672-35,535,507 INSM2
    nsv3904370copy number variation1nstd102humanBenign GRCh37 chr14: 35,997,555-36,004,713 , GRCh38.p12 chr14: 35,528,349-35,535,507 INSM2
    nsv3901334copy number variation1nstd102humanBenign GRCh37 chr14: 35,998,386-36,003,861 , GRCh38.p12 chr14: 35,529,180-35,534,655 INSM2
    nsv3909424copy number variation1nstd102humanBenign GRCh37 chr14: 36,002,650-36,004,238 , GRCh38.p12 chr14: 35,533,444-35,535,032 INSM2
    nsv4631709copy number variation1nstd183human GRCh37 chr14: 36,002,608-36,004,777 , GRCh38.p12 chr14: 35,533,402-35,535,571 INSM2
    nsv4416691copy number variation1nstd174human GRCh37 chr14: 36,002,608-36,004,777 , GRCh38.p12 chr14: 35,533,402-35,535,571 INSM2
    nsv1364998copy number variation1nstd122human NCBI36 chr14: 35,067,306-35,074,464 , GRCh37.p13 chr14: 35,997,555-36,004,713 , GRCh38.p12 chr14: 35,528,349-35,535,507 INSM2
    nsv1369724copy number variation4nstd122human NCBI36 chr14: 35,068,137-35,074,464 , GRCh37.p13 chr14: 35,998,386-36,004,713 , GRCh38.p12 chr14: 35,529,180-35,535,507 INSM2
    nsv1372465copy number variation8nstd122human NCBI36 chr14: 35,069,621-35,074,242 , GRCh37.p13 chr14: 35,999,870-36,004,491 , GRCh38.p12 chr14: 35,530,664-35,535,285 INSM2
    nsv1371552copy number variation2nstd122human NCBI36 chr14: 35,072,683-35,075,138 , GRCh37.p13 chr14: 36,002,932-36,005,387 , GRCh38.p12 chr14: 35,533,726-35,536,181 INSM2
    nsv1375446copy number variation117nstd122human NCBI36 chr14: 35,072,683-35,074,464 , GRCh37.p13 chr14: 36,002,932-36,004,713 , GRCh38.p12 chr14: 35,533,726-35,535,507 INSM2
    nsv1366697copy number variation3nstd122human NCBI36 chr14: 35,072,786-35,074,464 , GRCh37.p13 chr14: 36,003,035-36,004,713 , GRCh38.p12 chr14: 35,533,829-35,535,507 INSM2
    nsv1376352copy number variation21nstd122human NCBI36 chr14: 35,072,683-35,074,290 , GRCh37.p13 chr14: 36,002,932-36,004,539 , GRCh38.p12 chr14: 35,533,726-35,535,333 INSM2
    nsv1375607copy number variation59nstd122human NCBI36 chr14: 35,072,683-35,074,242 , GRCh37.p13 chr14: 36,002,932-36,004,491 , GRCh38.p12 chr14: 35,533,726-35,535,285 INSM2
    nsv1369464copy number variation2nstd122human NCBI36 chr14: 35,072,786-35,074,290 , GRCh37.p13 chr14: 36,003,035-36,004,539 , GRCh38.p12 chr14: 35,533,829-35,535,333 INSM2
    nsv1368072copy number variation1nstd122human NCBI36 chr14: 35,073,002-35,074,464 , GRCh37.p13 chr14: 36,003,251-36,004,713 , GRCh38.p12 chr14: 35,534,045-35,535,507 INSM2
    nsv1374130copy number variation1nstd122human NCBI36 chr14: 35,072,683-35,074,102 , GRCh37.p13 chr14: 36,002,932-36,004,351 , GRCh38.p12 chr14: 35,533,726-35,535,145 INSM2
    nsv1374246copy number variation1nstd122human NCBI36 chr14: 35,072,894-35,074,242 , GRCh37.p13 chr14: 36,003,143-36,004,491 , GRCh38.p12 chr14: 35,533,937-35,535,285 INSM2
    nsv1375332copy number variation4nstd122human NCBI36 chr14: 35,072,683-35,073,989 , GRCh37.p13 chr14: 36,002,932-36,004,238 , GRCh38.p12 chr14: 35,533,726-35,535,032 INSM2
    nsv1373121copy number variation1nstd122human NCBI36 chr14: 35,073,002-35,074,242 , GRCh37.p13 chr14: 36,003,251-36,004,491 , GRCh38.p12 chr14: 35,534,045-35,535,285 INSM2
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