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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5929390copy number variation1nstd209human GRCh38 chr19: 48,632,328-48,632,454 , GRCh37.p13 chr19: 49,135,585-49,135,711 DBP
    nsv5667352inversion1nstd207human GRCh38 chr19: 47,959,661-50,091,195 , GRCh37.p13 chr19: 48,462,918-50,594,452 , AP2A1, 145 more genes
    nsv5533205copy number variation1nstd206human GRCh38 chr19: 48,632,357-48,632,455 , GRCh37.p13 chr19: 49,135,614-49,135,712 DBP
    nsv5380243translocation1nstd200human GRCh38 chr19: 843,261-843,261 , GRCh38 chr19: 48,631,180-48,631,180 , GRCh37.p13 chr19: 49,134,437-49,134,437 , GRCh37.p13 chr19: 843,261-843,261 PRTN3, DBP
    nsv5020924copy number variation1nstd200human GRCh38 chr19: 48,636,978-48,637,101 , GRCh37.p13 chr19: 49,140,235-49,140,358 SEC1P, DBP, 1 more genes
    nsv4730038copy number variation1nstd102humanLikely pathogenic GRCh37 chr19: 48,854,319-49,430,535 , GRCh38.p12 chr19: 48,351,062-48,927,278 BCAT2, CA11, 32 more genes
    nsv4729755copy number variation1nstd102humanPathogenic GRCh37 chr19: 48,463,931-57,095,254 , GRCh38.p12 chr19: 47,960,674-56,583,886 SIGLEC5, MED25, 574 more genes
    nsv4685764copy number variation1nstd102humannot provided GRCh37 chr19: 47,939,842-54,626,871 , GRCh38.p12 chr19: 47,436,585-54,071,460 SNAR-G1, IRF3, 453 more genes
    nsv4676357copy number variation1nstd102humanPathogenic GRCh37 chr19: 44,738,088-53,621,561 , GRCh38.p12 chr19: 44,233,935-53,118,308 MIR4324, KLK9, 485 more genes
    nsv4619750copy number variation1nstd183human GRCh37 chr19: 48,873,011-49,196,722 , GRCh38.p12 chr19: 48,369,754-48,693,465 , DBP, 16 more genes
    nsv4457853copy number variation1nstd102humanUncertain significance GRCh37 chr19: 48,119,589-49,595,956 , GRCh38.p12 chr19: 47,616,332-49,092,699 DHDH, GRIN2D, 94 more genes
    nsv4457372copy number variation1nstd102humanPathogenic GRCh37 chr19: 28,271,106-49,213,832 , GRCh38.p12 chr19: 27,780,198-48,710,575 ZNF461, LOC101927572, 735 more genes
    nsv4376838copy number variation1nstd173human GRCh37 chr19: 48,462,617-51,107,899 , GRCh38.p12 chr19: 47,959,360-50,604,642 , LIN7B, 173 more genes
    nsv4321864inversion1nstd166human GRCh37.p13 chr19: 46,657,897-51,634,775 , GRCh38.p12 chr19: 46,154,640-51,131,518 , C5AR1, 288 more genes
    nsv4269578copy number variation1nstd166human GRCh37.p13 chr19: 49,135,614-49,135,719 , GRCh38.p12 chr19: 48,632,357-48,632,462 DBP
    nsv4260721copy number variation1nstd166human GRCh37.p13 chr19: 49,140,235-49,140,358 , GRCh38.p12 chr19: 48,636,978-48,637,101 CA11, DBP, 1 more genes
    nsv3924184copy number variation1nstd102humanUncertain significance GRCh37 chr19: 49,080,908-49,342,299 , GRCh38 chr19: 48,577,651-48,839,042 , NCBI36 chr19: 53,772,720-54,034,111 RNU6-317P, LOC105372432, 20 more genes
    nsv3919076copy number variation1nstd102humanPathogenic GRCh37 chr19: 48,432,832-59,083,573 , NCBI36 chr19: 53,124,644-63,775,385 , GRCh38 chr19: 47,929,575-58,572,206 KCNA7, ZNF28, 697 more genes
    nsv3918983copy number variation1nstd102humanPathogenic GRCh38 chr19: 46,658,791-49,050,450 , GRCh37 chr19: 47,162,048-49,553,707 , NCBI36 chr19: 51,853,888-54,245,519 LOC105372432, FTL, 121 more genes
    nsv3911950copy number variation1nstd102humanPathogenic GRCh37 chr19: 48,411,797-59,051,332 , NCBI36 chr19: 53,103,609-63,743,144 , GRCh38 chr19: 47,908,540-58,539,965 LOC107987270, MIR6799, 694 more genes
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