U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Links from Gene

Items: 1 to 20 of 415

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095478copy number variation1nstd102humanUncertain significance GRCh37 chr19: 33,167,170-36,643,309 , GRCh38.p12 chr19: 32,676,264-36,152,407 NFKBID, LRP3, 141 more genes
    nsv7074671inversion1nstd229human GRCh38 chr19: 33,126,299-36,006,645 , GRCh37.p13 chr19: 33,617,205-36,497,547 , ZNF30, 120 more genes
    nsv7074279inversion1nstd229human GRCh38 chr19: 33,135,428-36,017,833 , GRCh37.p13 chr19: 33,626,334-36,508,735 , PSENEN, 122 more genes
    nsv7016825copy number variation1nstd229human GRCh38 chr19: 34,254,201-34,255,800 , GRCh37.p13 chr19: 34,745,106-34,746,705 GARRE1
    nsv7013492copy number variation1nstd229human GRCh38 chr19: 34,276,801-34,287,900 , GRCh37.p13 chr19: 34,767,706-34,778,805 GARRE1
    nsv7013231copy number variation1nstd229human GRCh38 chr19: 34,350,611-34,374,924 , GRCh37.p13 chr19: 34,841,516-34,865,829 GPI, GARRE1
    nsv7008965copy number variation1nstd229human GRCh38 chr19: 34,325,427-34,510,322 , GRCh37.p13 chr19: 34,816,332-35,001,227 RN7SL154P, WTIP, 4 more genes
    nsv7007759copy number variation1nstd229human GRCh38 chr19: 34,332,849-34,337,794 , GRCh37.p13 chr19: 34,823,754-34,828,699 GARRE1
    nsv7005713copy number variation1nstd229human GRCh38 chr19: 33,458,650-39,721,746 , GRCh37.p13 chr19: 33,949,556-40,212,386 , TYROBP, 259 more genes
    nsv7002879copy number variation1nstd229human GRCh38 chr19: 34,284,335-34,286,432 , GRCh37.p13 chr19: 34,775,240-34,777,337 GARRE1
    nsv7002053copy number variation1nstd229human GRCh38 chr19: 34,288,901-34,289,456 , GRCh37.p13 chr19: 34,779,806-34,780,361 GARRE1
    nsv7001397copy number variation1nstd229human GRCh38 chr19: 34,290,483-34,295,313 , GRCh37.p13 chr19: 34,781,388-34,786,218 GARRE1, RPL29P33
    nsv6637967copy number variation1nstd102humanUncertain significance GRCh37 chr19: 34,737,425-34,779,637 , GRCh38.p12 chr19: 34,246,520-34,288,732 , GRCh38.p12 chr19|NW_003315963.1: 101,436-143,646 GARRE1
    nsv6599897inversion1nstd223human GRCh38 chr19: 34,334,791-34,335,728 , GRCh37.p13 chr19: 34,825,696-34,826,633 GARRE1
    nsv6598934inversion1nstd223human GRCh38 chr19: 34,289,596-34,290,905 , GRCh37.p13 chr19: 34,780,501-34,781,810 GARRE1
    nsv6598690inversion1nstd223human GRCh38 chr19: 34,262,970-34,263,615 , GRCh37.p13 chr19: 34,753,875-34,754,520 GARRE1
    nsv6597742inversion1nstd223human GRCh38 chr19: 34,258,149-34,258,542 , GRCh37.p13 chr19: 34,749,054-34,749,447 GARRE1
    nsv6597398inversion1nstd223human GRCh38 chr19: 34,328,286-34,328,622 , GRCh37.p13 chr19: 34,819,191-34,819,527 GARRE1
    nsv6597300inversion1nstd223human GRCh38 chr19: 34,289,915-34,290,516 , GRCh37.p13 chr19: 34,780,820-34,781,421 GARRE1
    nsv6597140inversion1nstd223human GRCh38 chr19: 34,278,430-34,278,725 , GRCh37.p13 chr19: 34,769,335-34,769,630 GARRE1
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Find related data

    Support Center