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Items: 1 to 20 of 607

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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
    nsv7074244inversion1nstd229human GRCh38 chr22: 42,546,504-42,560,066 , GRCh37.p13 chr22: 42,942,510-42,956,072 SERHL2
    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
    nsv7062397inversion1nstd229human GRCh38 chr22: 42,529,195-42,554,156 , GRCh37.p13 chr22: 42,925,201-42,950,162 SERHL2
    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
    nsv7037075copy number variation1nstd229human GRCh38 chr22: 42,567,874-42,569,027 , GRCh37.p13 chr22: 42,963,880-42,965,033 SERHL2, RNU6-513P
    nsv7028449copy number variation1nstd229human GRCh38 chr22: 42,568,190-42,572,832 , GRCh37.p13 chr22: 42,964,196-42,968,838 RRP7BP, SERHL2, 1 more genes
    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
    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
    nsv7019780copy number variation1nstd229human GRCh38 chr22: 42,569,445-42,569,632 , GRCh37.p13 chr22: 42,965,451-42,965,638 SERHL2, RNU6-513P
    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
    nsv6635662copy number variation1nstd227human GRCh38.p12 chr22: 42,521,148-42,585,161 , GRCh37 chr22: 42,917,154-42,981,167 POLDIP3, RRP7BP, 3 more genes
    nsv6627479copy number variation1nstd224human GRCh37 chr22: 42,919,010-42,992,359 , GRCh38.p12 chr22: 42,523,004-42,596,353 POLDIP3, SERHL2, 3 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
    nsv6627288copy number variation1nstd224human GRCh37 chr22: 42,917,154-42,968,465 , GRCh38.p12 chr22: 42,521,148-42,572,459 RRP7BP, RNU6-513P, 2 more genes
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