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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
    nsv7074271inversion1nstd229human GRCh38 chr22: 42,494,408-42,550,313 , GRCh37.p13 chr22: 42,890,414-42,946,319 RRP7A, SERHL, 1 more genes
    nsv7069304inversion1nstd229human GRCh38 chr22: 41,294,727-42,750,704 , GRCh37.p13 chr22: 41,690,731-43,146,710 SERHL2, CSDC2, 63 more genes
    nsv7066611inversion1nstd229human GRCh38 chr22: 42,490,849-42,573,416 , GRCh37.p13 chr22: 42,886,855-42,969,422 RRP7BP, SERHL, 5 more genes
    nsv7062301inversion1nstd229human GRCh38 chr22: 42,511,285-42,551,193 , GRCh37.p13 chr22: 42,907,291-42,947,199 RRP7A, SERHL
    nsv7061959inversion1nstd229human GRCh38 chr22: 36,818,005-44,993,640 , GRCh37.p13 chr22: 37,214,049-45,389,520 SMIM45, A4GALT, 271 more genes
    nsv7058827inversion1nstd229human GRCh38 chr22: 42,518,031-42,753,421 , GRCh37.p13 chr22: 42,914,037-43,149,427 CYB5R3, A4GALT, 8 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
    nsv7037744copy number variation1nstd229human GRCh38 chr22: 42,520,034-42,528,761 , GRCh37.p13 chr22: 42,916,040-42,924,767 RRP7A
    nsv7035639copy number variation1nstd229human GRCh38 chr22: 42,520,251-42,533,557 , GRCh37.p13 chr22: 42,916,257-42,929,563 RRP7A
    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
    nsv7024601copy number variation1nstd229human GRCh38 chr22: 42,520,201-42,524,800 , GRCh37.p13 chr22: 42,916,207-42,920,806 RRP7A
    nsv7020273copy number variation1nstd229human GRCh38 chr22: 42,480,674-42,589,000 , GRCh37.p13 chr22: 42,876,680-42,985,006 RRP7A, SERHL, 6 more genes
    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
    nsv6637527copy number variation1nstd102humanUncertain significance GRCh37 chr22: 42,765,874-43,059,475 , GRCh38.p12 chr22: 42,369,868-42,663,469 SERHL2, SERHL, 11 more genes
    nsv6635228copy number variation1nstd227human GRCh38.p12 chr22: 42,459,271-42,523,004 , GRCh37 chr22: 42,855,277-42,919,010 RRP7A, SERHL, 1 more genes
    nsv6627478copy number variation4nstd224human GRCh37 chr22: 42,908,938-42,968,465 , GRCh38.p12 chr22: 42,512,932-42,572,459 RRP7A, RRP7BP, 4 more genes
    nsv6627477copy number variation1nstd224human GRCh37 chr22: 42,876,604-42,950,033 , GRCh38.p12 chr22: 42,480,598-42,554,027 LOC101927372, SERHL2, 2 more genes
    nsv6627418copy number variation1nstd224human GRCh37 chr22: 42,908,938-42,998,017 , GRCh38.p12 chr22: 42,512,932-42,602,011 RRP7A, POLDIP3, 5 more genes
    nsv6627417copy number variation2nstd224human GRCh37 chr22: 42,908,938-42,919,010 , GRCh38.p12 chr22: 42,512,932-42,523,004 RRP7A, SERHL
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