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 127

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5288700copy number variation1nstd204human GRCh38.p13 chr19: 54,205,753-54,210,852 , GRCh37.p13 chr19|NW_004166865.1: 180,120-185,219 RPS9
    nsv5021325copy number variation1nstd200human GRCh38 chr19: 54,207,949-54,211,697 , GRCh37.p13 chr19|NW_004166865.1: 182,316-186,064 RPS9
    nsv5021324copy number variation1nstd200human GRCh38 chr19: 54,205,087-54,206,215 , GRCh37.p13 chr19|NW_004166865.1: 179,454-180,582 RPS9
    nsv4861338copy number variation1nstd200human GRCh37 chr19: 54,708,955-54,710,083 , GRCh38.p12 chr19|NW_003571057.2: 180,069-181,197 , GRCh38.p12 chr19|NW_003571060.1: 180,056-181,186 , GRCh38.p12 chr19|NW_003571058.2: 180,069-181,197 , GRCh38.p12 chr19|NW_003571054.1: 179,886-181,014 , GRCh38.p12 chr19|NW_003571061.2: 180,069-181,197 , GRCh38.p12 chr19|NW_003571059.2: 180,069-181,197 , GRCh38.p12 chr19|NW_003571055.2: 180,069-181,197 , GRCh38.p12 chr19: 54,205,087-54,206,215 , GRCh38.p12 chr19|NT_187693.1: 180,069-181,197 , GRCh38.p12 chr19|NW_003571056.2: 180,069-181,197 RPS9
    nsv4730034copy number variation1nstd102humanUncertain significance GRCh37 chr19: 54,334,195-56,434,037 , GRCh38.p12 chr19: 53,830,941-55,922,671 , GRCh38.p12 chr19|NT_187693.1: 1-1,066,800 , GRCh38.p12 chr19|NW_003571057.2: 1-1,091,841 , GRCh38.p12 chr19|NW_003571058.2: 1-1,066,390 , GRCh38.p12 chr19|NW_003571056.2: 1-1,064,304 KIR3DP1, NLRP9, 133 more genes
    nsv4729999copy number variation1nstd102humanUncertain significance GRCh37 chr19: 54,659,105-54,916,280 , GRCh38.p12 chr19|NT_187693.1: 134,805-387,394 , GRCh38.p12 chr19|NW_003571054.1: 130,217-309,793 , GRCh38.p12 chr19: 54,155,367-54,404,676 , GRCh38.p12 chr19|NW_003571061.2: 130,218-361,078 , GRCh38.p12 chr19|NW_003571060.1: 130,218-309,667 , GRCh38.p12 chr19|NW_003571055.2: 134,805-385,761 RPS9, MIR4752, 23 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
    nsv4676386copy number variation1nstd102humanUncertain significance GRCh37 chr19: 54,474,844-55,181,741 , GRCh38.p12 chr19|NT_187693.1: 134,805-652,855 , GRCh38.p12 chr19: 54,071,461-54,670,290 , GRCh38.p12 chr19|NW_003571060.1: 1-575,172 , GRCh38.p12 chr19|NW_003571061.2: 1-396,794 , GRCh38.p12 chr19|NW_003571055.2: 1-394,095 , GRCh38.p12 chr19|NW_003571054.1: 1-576,693 OSCAR, CNOT3, 48 more genes
    nsv4676358copy number variation1nstd102humanUncertain significance GRCh37 chr19: 54,701,333-55,536,206 , GRCh38.p12 chr19|NW_003571058.2: 172,447-1,006,910 , GRCh38.p12 chr19|NW_003571059.2: 172,447-943,203 , GRCh38.p12 chr19|NW_003571060.1: 172,438-927,620 , GRCh38.p12 chr19|NW_003571054.1: 172,267-928,236 , GRCh38.p12 chr19|NW_003571061.2: 172,447-736,999 , GRCh38.p12 chr19|NW_003571057.2: 172,447-1,032,361 , GRCh38.p12 chr19|NW_003571056.2: 172,447-1,004,824 , GRCh38.p12 chr19: 54,197,469-54,911,985 , GRCh38.p12 chr19|NT_187693.1: 172,447-894,467 , GRCh38.p12 chr19|NW_003571055.2: 172,447-670,040 LILRA1, KIR2DL4, 65 more genes
    nsv4626449copy number variation1nstd183human GRCh37 chr19: 54,700,885-54,705,019 , GRCh38.p12 chr19: 54,197,021-54,201,151 , GRCh38.p12 chr19|NW_003571057.2: 171,999-176,133 , GRCh38.p12 chr19|NW_003571060.1: 171,990-176,123 , GRCh38.p12 chr19|NW_003571054.1: 171,819-175,950 , GRCh38.p12 chr19|NW_003571061.2: 171,999-176,133 , GRCh38.p12 chr19|NW_003571059.2: 171,999-176,133 , GRCh38.p12 chr19|NW_003571055.2: 171,999-176,133 , GRCh38.p12 chr19|NW_003571058.2: 171,999-176,133 , GRCh38.p12 chr19|NT_187693.1: 171,999-176,133 , GRCh38.p12 chr19|NW_003571056.2: 171,999-176,133 RPS9
    nsv4626430copy number variation1nstd183human GRCh37 chr19: 54,657,877-54,741,319 , GRCh38.p12 chr19: 54,154,140-54,237,443 , GRCh38.p12 chr19|NW_003571061.2: 128,990-195,632 , GRCh38.p12 chr19|NW_003571059.2: 128,990-195,632 , GRCh38.p12 chr19|NW_003571058.2: 128,990-195,632 , GRCh38.p12 chr19|NW_003571060.1: 128,990-212,432 , GRCh38.p12 chr19|NW_003571056.2: 128,990-195,632 , GRCh38.p12 chr19|NW_003571055.2: 134,805-195,632 , GRCh38.p12 chr19|NW_003571054.1: 128,990-212,219 , GRCh38.p12 chr19|NT_187693.1: 134,805-212,433 , GRCh38.p12 chr19|NW_003571057.2: 128,990-195,632 , LOC107987425, 17 more genes
    nsv4623081copy number variation2nstd183human GRCh37 chr19: 54,711,350-54,777,790 , GRCh38.p12 chr19: 54,207,482-54,273,936 , GRCh38.p12 chr19|NT_187693.1: 182,464-248,904 , GRCh38.p12 chr19|NW_003571061.2: 182,464-248,930 , GRCh38.p12 chr19|NW_003571060.1: 182,453-248,918 , GRCh38.p12 chr19|NW_003571054.1: 182,281-248,675 LILRB2, RPS9, 12 more genes
    nsv4623004copy number variation1nstd183human GRCh37 chr19: 54,681,950-54,723,239 , GRCh38.p12 chr19|NW_003571061.2: 153,064-194,353 , GRCh38.p12 chr19|NW_003571059.2: 153,064-194,353 , GRCh38.p12 chr19|NW_003571055.2: 153,064-194,353 , GRCh38.p12 chr19|NW_003571054.1: 153,022-194,170 , GRCh38.p12 chr19: 54,178,233-54,219,370 , GRCh38.p12 chr19|NT_187693.1: 153,064-194,353 , GRCh38.p12 chr19|NW_003571057.2: 153,064-194,353 , GRCh38.p12 chr19|NW_003571060.1: 153,027-194,356 , GRCh38.p12 chr19|NW_003571058.2: 153,064-194,353 , GRCh38.p12 chr19|NW_003571056.2: 153,064-194,353 , LOC107987425, 10 more genes
    nsv4621672copy number variation2nstd183human GRCh37 chr19: 54,695,874-54,849,275 , GRCh38.p12 chr19: 54,192,023-54,338,004 , GRCh38.p12 chr19|NT_187693.1: 166,988-320,389 , GRCh38.p12 chr19|NW_003571060.1: 166,987-253,362 , GRCh38.p12 chr19|NW_003571055.2: 166,988-319,351 , GRCh38.p12 chr19|NW_003571054.1: 166,820-309,793 , GRCh38.p12 chr19|NW_003571061.2: 166,988-319,505 LAIR1, LILRA5, 19 more genes
    nsv4383528copy number variation1nstd173human GRCh37 chr19: 54,663,509-54,730,309 , GRCh38.p12 chr19: 54,159,771-54,226,436 , GRCh38.p12 chr19|NT_187693.1: 134,805-201,423 , GRCh38.p12 chr19|NW_003571061.2: 134,622-195,632 , GRCh38.p12 chr19|NW_003571057.2: 134,622-195,632 , GRCh38.p12 chr19|NW_003571058.2: 134,622-195,632 , GRCh38.p12 chr19|NW_003571059.2: 134,622-195,632 , GRCh38.p12 chr19|NW_003571060.1: 134,622-201,421 , GRCh38.p12 chr19|NW_003571056.2: 134,622-195,632 , GRCh38.p12 chr19|NW_003571055.2: 134,805-195,632 , GRCh38.p12 chr19|NW_003571054.1: 134,621-201,236 , LOC107987425, 13 more genes
    nsv4374650copy number variation1nstd173human GRCh37 chr19: 54,711,497-54,752,217 , GRCh38.p12 chr19: 54,207,629-54,248,358 , GRCh38.p12 chr19|NT_187693.1: 182,611-223,331 , GRCh38.p12 chr19|NW_003571061.2: 182,611-223,362 , GRCh38.p12 chr19|NW_003571060.1: 182,600-223,326 , GRCh38.p12 chr19|NW_003571054.1: 182,428-223,093 LOC100421130, LILRB5, 8 more genes
    nsv4372936copy number variation1nstd173human GRCh37 chr19: 54,710,673-54,784,920 , GRCh38.p12 chr19: 54,206,805-54,281,065 , GRCh38.p12 chr19|NT_187693.1: 181,787-256,034 , GRCh38.p12 chr19|NW_003571061.2: 181,787-256,059 , GRCh38.p12 chr19|NW_003571060.1: 181,776-253,362 , GRCh38.p12 chr19|NW_003571054.1: 181,604-255,804 LOC100421130, LAIR1, 13 more genes
    nsv4271954copy number variation1nstd166human GRCh37.p13 chr19: 54,688,892-54,704,296 , GRCh38.p12 chr19|NW_003571061.2: 160,006-175,410 , GRCh38.p12 chr19|NW_003571058.2: 160,006-175,410 , GRCh38.p12 chr19|NW_003571060.1: 159,968-175,401 , GRCh38.p12 chr19|NW_003571056.2: 160,006-175,410 , GRCh38.p12 chr19|NW_003571054.1: 159,801-175,228 , GRCh38.p12 chr19|NW_003571059.2: 160,006-175,410 , GRCh38.p12 chr19|NW_003571055.2: 160,006-175,410 , GRCh38.p12 chr19: 54,185,008-54,200,429 , GRCh38.p12 chr19|NT_187693.1: 160,006-175,410 , GRCh38.p12 chr19|NW_003571057.2: 160,006-175,410 TSEN34, RPS9, 1 more genes
    nsv4255228copy number variation1nstd166human GRCh37.p13 chr19: 54,702,000-54,707,000 , GRCh38.p12 chr19: 54,198,135-54,203,132 , GRCh38.p12 chr19|NW_003571061.2: 173,114-178,114 , GRCh38.p12 chr19|NW_003571058.2: 173,114-178,114 , GRCh38.p12 chr19|NW_003571056.2: 173,114-178,114 , GRCh38.p12 chr19|NT_187693.1: 173,114-178,114 , GRCh38.p12 chr19|NW_003571057.2: 173,114-178,114 , GRCh38.p12 chr19|NW_003571060.1: 173,106-178,104 , GRCh38.p12 chr19|NW_003571059.2: 173,114-178,114 , GRCh38.p12 chr19|NW_003571055.2: 173,114-178,114 , GRCh38.p12 chr19|NW_003571054.1: 172,933-177,931 RPS9
    nsv3968928copy number variation1nstd168human GRCh38 chr19: 54,205,567-54,304,611 , GRCh37.p13 chr19|NW_004166865.1: 179,934-278,978 LILRB3, LILRA6, 8 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