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 107

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5869650copy number variation2nstd209human GRCh38 chr19: 44,667,511-44,670,143 , GRCh37.p13 chr19: 45,170,779-45,173,415 CEACAM19, CEACAM16-AS1
    nsv4853034copy number variation1nstd200human GRCh37 chr19: 45,174,337-45,194,013 , GRCh38.p12 chr19: 44,671,065-44,690,741 LOC107985306, CEACAM16-AS1, 1 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
    nsv4625911copy number variation1nstd183human GRCh37 chr19: 45,176,041-45,287,600 , GRCh38.p12 chr19: 44,672,769-44,784,343 BCL3, CBLC, 5 more genes
    nsv4623840copy number variation1nstd183human GRCh37 chr19: 45,020,272-45,216,013 , GRCh38.p12 chr19: 44,516,211-44,712,744 PVR, CEACAM19, 7 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
    nsv4436634complex substitution1nstd102humanUncertain significance GRCh38.p12 chr19: 43,997,366-44,819,487 , GRCh37 chr19: 44,501,518-45,322,744 BCL3, BCAM, 34 more genes
    nsv3957016copy number variation1nstd168human GRCh38 chr19: 44,663,384-44,726,466 , GRCh37.p13 chr19: 45,166,651-45,229,729 PVR, CEACAM16-AS1, 3 more genes
    nsv3904885copy number variation1nstd102humanPathogenic GRCh37 chr19: 68,029-59,110,290 , GRCh38.p12 chr19: 68,029-58,598,923 ZNF321P, ZNF861P, 2443 more genes
    nsv3903203copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,912-59,097,160 , GRCh38.p12 chr19: 260,912-58,585,793 BABAM1, BEST2, 2426 more genes
    nsv3903092copy number variation2nstd102humanPathogenic GRCh37 chr19: 260,912-58,956,888 , GRCh38.p12 chr19: 260,912-58,445,521 LENG8, SYDE1, 2408 more genes
    nsv3891669copy number variation1nstd102humanPathogenic GRCh37 chr19: 43,013,365-47,241,534 , GRCh38.p12 chr19: 42,509,213-46,738,277 MIR320E, BCL3, 189 more genes
    nsv3890841copy number variation1nstd102humanUncertain significance GRCh37 chr19: 44,300,416-45,639,540 , GRCh38.p12 chr19: 43,796,264-45,136,282 ZNF225, ZNF296, 57 more genes
    nsv3168446copy number variation1nstd158human GRCh37 chr19: 35,445,908-45,506,757 , GRCh38.p12 chr19: 34,955,004-45,003,499 , ACTN4, 449 more genes
    nsv3165043copy number variation1nstd151human GRCh37 chr19: 45,153,078-45,183,611 , GRCh38.p12 chr19: 44,649,806-44,680,339 MIR4531, PVR, 2 more genes
    nsv3163629copy number variation1nstd151human GRCh37 chr19: 45,161,027-45,184,589 , GRCh38.p12 chr19: 44,657,759-44,681,317 CEACAM16-AS1, CEACAM19, 1 more genes
    nsv3160305copy number variation1nstd151human GRCh37 chr19: 44,890,631-45,262,103 , GRCh38.p12 chr19: 44,386,469-44,758,846 IGSF23, CEACAM16, 13 more genes
    nsv3160097copy number variation1nstd151human GRCh37 chr19: 45,153,078-45,179,698 , GRCh38.p12 chr19: 44,649,806-44,676,426 PVR, MIR4531, 2 more genes
    nsv2757532copy number variation1nstd130human GRCh37 chr19: 266,034-54,723,310 , GRCh38.p12 chr19: 266,034-54,071,460 , BABAM1, 2197 more genes
    nsv2752158copy number variation1nstd130human GRCh37 chr19: 289,244-58,996,454 , GRCh38.p12 chr19: 289,244-58,485,087 , NFKBIB, 2456 more genes
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Recent activity

    Clear Turn Off Turn On

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

    See more...
    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
    Support Center