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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096314copy number variation1nstd102humanPathogenic GRCh37 chr22: 42,456,283-43,089,957 , GRCh38.p12 chr22: 42,060,279-42,693,951 SERHL2, POLDIP3, 28 more genes
    nsv7071105inversion1nstd229human GRCh38 chr22: 42,232,703-42,258,964 , GRCh37.p13 chr22: 42,628,709-42,654,970 TCF20
    nsv7069304inversion1nstd229human GRCh38 chr22: 41,294,727-42,750,704 , GRCh37.p13 chr22: 41,690,731-43,146,710 SERHL2, CSDC2, 63 more genes
    nsv7064830inversion1nstd229human GRCh38 chr22: 42,251,840-42,258,855 , GRCh37.p13 chr22: 42,647,846-42,654,861 TCF20
    nsv7064182inversion1nstd229human GRCh38 chr22: 42,200,845-42,201,072 , GRCh37.p13 chr22: 42,596,851-42,597,078 TCF20
    nsv7061959inversion1nstd229human GRCh38 chr22: 36,818,005-44,993,640 , GRCh37.p13 chr22: 37,214,049-45,389,520 SMIM45, A4GALT, 271 more genes
    nsv7058666inversion1nstd229human GRCh38 chr22: 39,066,437-42,707,681 , GRCh37.p13 chr22: 39,462,442-43,103,687 LOC101927344, ATF4, 128 more genes
    nsv7038060copy number variation1nstd229human GRCh38 chr22: 42,185,823-42,191,513 , GRCh37.p13 chr22: 42,581,829-42,587,519 TCF20
    nsv7036534copy number variation1nstd229human GRCh38 chr22: 42,231,236-42,233,940 , GRCh37.p13 chr22: 42,627,242-42,629,946 TCF20
    nsv7032574copy number variation1nstd229human GRCh38 chr22: 42,038,695-42,212,931 , GRCh37.p13 chr22: 42,434,699-42,608,937 TCF20, PHETA2, 13 more genes
    nsv7029905copy number variation1nstd229human GRCh38 chr22: 42,216,969-42,222,916 , GRCh37.p13 chr22: 42,612,975-42,618,922 TCF20
    nsv7028488copy number variation1nstd229human GRCh38 chr22: 42,231,678-42,232,274 , GRCh37.p13 chr22: 42,627,684-42,628,280 TCF20
    nsv7028079copy number variation1nstd229human GRCh38 chr22: 42,267,086-42,267,964 , GRCh37.p13 chr22: 42,663,092-42,663,970 TCF20, OGFRP1
    nsv7027741copy number variation1nstd229human GRCh38 chr22: 39,432,386-49,047,389 , GRCh37.p13 chr22: 39,828,391-49,443,201 LOC105373064, ACO2, 233 more genes
    nsv7026107copy number variation1nstd229human GRCh38 chr22: 42,195,601-42,198,400 , GRCh37.p13 chr22: 42,591,607-42,594,406 TCF20
    nsv7025345copy number variation1nstd229human GRCh38 chr22: 42,175,317-42,175,931 , GRCh37.p13 chr22: 42,571,323-42,571,937 TCF20
    nsv7024344copy number variation1nstd229human GRCh38 chr22: 42,161,933-42,164,590 , GRCh37.p13 chr22: 42,557,939-42,560,596 TCF20
    nsv7019708copy number variation1nstd229human GRCh38 chr22: 42,238,882-42,243,368 , GRCh37.p13 chr22: 42,634,888-42,639,374 TCF20
    nsv7018720copy number variation1nstd229human GRCh38 chr22: 42,267,114-42,268,037 , GRCh37.p13 chr22: 42,663,120-42,664,043 OGFRP1, TCF20
    nsv6638049copy number variation1nstd102humanUncertain significance GRCh37 chr22: 42,603,838-42,942,949 , GRCh38.p12 chr22: 42,207,832-42,546,943 LOC101927372, SERHL, 6 more genes
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