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Items: 1 to 20 of 522

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098190copy number variation1nstd102humanUncertain significance GRCh37 chr8: 98,358,247-106,815,766 , GRCh38.p12 chr8: 97,346,019-105,803,538 RNU6-914P, RPL30, 159 more genes
    nsv7073376inversion1nstd229human GRCh38 chr8: 99,051,852-103,793,725 , GRCh37.p13 chr8: 100,064,080-104,805,953 RNU4-83P, RN7SL563P, 102 more genes
    nsv7071870inversion1nstd229human GRCh38 chr8: 99,825,313-99,969,249 , GRCh37.p13 chr8: 100,837,541-100,981,477 VPS13B, RGS22, 1 more genes
    nsv7066903inversion1nstd229human GRCh38 chr8: 100,019,756-100,024,163 , GRCh37.p13 chr8: 101,031,984-101,036,391 RGS22
    nsv7066312inversion1nstd229human GRCh38 chr8: 100,051,381-100,051,507 , GRCh37.p13 chr8: 101,063,609-101,063,735 RGS22
    nsv6858022copy number variation1nstd229human GRCh38 chr8: 100,093,901-100,262,000 , GRCh37.p13 chr8: 101,106,129-101,274,228 UFM1P3, RNF19A, 5 more genes
    nsv6856338copy number variation1nstd229human GRCh38 chr8: 100,044,112-100,056,372 , GRCh37.p13 chr8: 101,056,340-101,068,600 RGS22
    nsv6853073copy number variation1nstd229human GRCh38 chr8: 100,107,061-100,114,355 , GRCh37.p13 chr8: 101,119,289-101,126,583 RGS22
    nsv6852528copy number variation1nstd229human GRCh38 chr8: 100,100,095-100,105,622 , GRCh37.p13 chr8: 101,112,323-101,117,850 RGS22
    nsv6851814copy number variation1nstd229human GRCh38 chr8: 100,026,655-100,027,868 , GRCh37.p13 chr8: 101,038,883-101,040,096 RGS22
    nsv6851398copy number variation1nstd229human GRCh38 chr8: 99,997,757-99,997,850 , GRCh37.p13 chr8: 101,009,985-101,010,078 RGS22
    nsv6851182copy number variation1nstd229human GRCh38 chr8: 100,071,468-100,071,866 , GRCh37.p13 chr8: 101,083,696-101,084,094 RGS22
    nsv6848861copy number variation1nstd229human GRCh38 chr8: 100,041,140-100,044,171 , GRCh37.p13 chr8: 101,053,368-101,056,399 RGS22
    nsv6847395copy number variation1nstd229human GRCh38 chr8: 100,007,701-100,261,900 , GRCh37.p13 chr8: 101,019,929-101,274,128 UFM1P3, RNF19A, 5 more genes
    nsv6846074copy number variation1nstd229human GRCh38 chr8: 100,072,806-100,075,770 , GRCh37.p13 chr8: 101,085,034-101,087,998 RGS22
    nsv6845067copy number variation1nstd229human GRCh38 chr8: 100,039,654-100,040,207 , GRCh37.p13 chr8: 101,051,882-101,052,435 RGS22
    nsv6842121copy number variation1nstd229human GRCh38 chr8: 100,047,071-100,051,671 , GRCh37.p13 chr8: 101,059,299-101,063,899 RGS22
    nsv6841780copy number variation1nstd229human GRCh38 chr8: 100,010,343-100,084,166 , GRCh37.p13 chr8: 101,022,571-101,096,394 RGS22
    nsv6839243copy number variation1nstd229human GRCh38 chr8: 100,087,368-100,096,758 , GRCh37.p13 chr8: 101,099,596-101,108,986 RGS22
    nsv6637993copy number variation1nstd102humanUncertain significance GRCh37 chr8: 100,791,384-101,278,033 , GRCh38.p12 chr8: 99,779,156-100,265,805 RNF19A, POLR2K, 8 more genes
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