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 152

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5604108copy number variation1nstd207human GRCh38 chr19: 54,712,104-54,712,334 , GRCh37.p13 chr19|NW_004166865.1: 686,471-686,701 LILRP2
    nsv5595147copy number variation1nstd207human GRCh38 chr19: 54,711,199-54,712,216 , GRCh37.p13 chr19|NW_004166865.1: 685,566-686,583 LILRP2
    nsv5587622copy number variation1nstd207human GRCh38 chr19: 54,711,547-54,711,600 , GRCh37.p13 chr19|NW_004166865.1: 685,914-685,967 LILRP2
    nsv5587349copy number variation1nstd207human GRCh38 chr19: 54,711,695-54,711,974 , GRCh37.p13 chr19|NW_004166865.1: 686,062-686,341 LILRP2
    nsv5532198copy number variation1nstd206human GRCh38 chr19: 54,711,752-54,712,356 , GRCh37.p13 chr19|NW_004166865.1: 686,119-686,723 LILRP2
    nsv5292606copy number variation1nstd204human GRCh38.p13 chr19: 54,711,259-54,716,029 , GRCh37.p13 chr19|NW_004166865.1: 685,626-690,396 LILRP2
    nsv5288175copy number variation1nstd204human GRCh38.p13 chr19: 54,711,359-54,716,629 , GRCh37.p13 chr19|NW_004166865.1: 685,726-690,996 LILRP2
    nsv5021351copy number variation1nstd200human GRCh38 chr19: 54,711,348-54,713,723 , GRCh37.p13 chr19|NW_004166865.1: 685,715-688,090 LILRP2
    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
    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
    nsv4684371copy number variation1nstd102humanUncertain significance GRCh38 chr19|NT_187693.1: 499,836-894,467 , NCBI36 chr19: 59,720,534-60,374,830 , GRCh37 chr19: 55,028,722-55,683,018 KIR2DL4, LILRA2, 24 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
    nsv4655359copy number variation1nstd186human GRCh37 chr19: 55,223,330-55,223,958 , GRCh38.p12 chr19|NT_187693.1: 694,444-695,072 LILRP2
    nsv4536394copy number variation1nstd166human GRCh37.p13 chr19: 55,054,999-55,564,000 , GRCh38.p12 chr19|NW_003571059.2: 705,634-970,997 , GRCh38.p12 chr19|NW_003571055.2: 399,097-697,834 , GRCh38.p12 chr19|NT_187693.1: 526,113-894,467 , GRCh38.p12 chr19|NW_003571061.2: 363,080-764,793 , GRCh38.p12 chr19|NW_003571060.1: 448,507-955,414 , GRCh38.p12 chr19|NT_187675.1: 4-282,224 , GRCh38.p12 chr19|NW_016107303.1: 1-293,522 , GRCh38.p12 chr19: 54,543,790-54,911,985 , GRCh38.p12 chr19|NW_003571054.1: 449,989-956,030 , LILRA2, 45 more genes
    nsv4534860copy number variation1nstd166human GRCh37.p13 chr19: 55,223,330-55,223,958 , GRCh38.p12 chr19|NT_187693.1: 694,444-695,072 LILRP2
    nsv4436654complex substitution1nstd102humanUncertain significance GRCh37 chr19: 55,143,156-55,294,969 , GRCh38.p12 chr19|NT_187693.1: 614,270-766,083 KIR2DL1, KIR2DL3, 10 more genes
    nsv4436309complex substitution1nstd102humanUncertain significance GRCh38.p12 chr19: 54,250,888-54,911,985 , GRCh37 chr19: 54,754,752-55,624,113 , GRCh38.p12 chr19|NW_003571055.2: 256,634-729,520 , GRCh38.p12 chr19|NW_003571061.2: 225,892-796,479 , GRCh38.p12 chr19|NW_003571060.1: 225,856-987,100 , GRCh38.p12 chr19|NW_003571054.1: 225,623-987,716 , GRCh38.p12 chr19|NT_187693.1: 225,866-894,467 FCAR, KIR2DL1, 54 more genes
    nsv4427822copy number variation1nstd174human GRCh37 chr19: 55,225,045-55,379,503 , GRCh38.p12 chr19|NT_187693.1: 696,159-850,617 RNU6-222P, KIR3DL3, 10 more genes
    nsv4414355copy number variation1nstd174human GRCh37 chr19: 54,983,659-55,605,756 , GRCh38.p12 chr19|NW_003571060.1: 377,167-987,100 , GRCh38.p12 chr19|NW_003571055.2: 399,097-729,520 , GRCh38.p12 chr19|NW_003571054.1: 378,926-987,716 , GRCh38.p12 chr19: 54,472,514-54,911,985 , GRCh38.p12 chr19|NT_187693.1: 454,773-894,467 , GRCh38.p12 chr19|NW_003571061.2: 363,080-796,479 , KIR2DP1, 41 more genes
    nsv4262521copy number variation1nstd166human GRCh37.p13 chr19: 55,224,409-55,224,470 , GRCh38.p12 chr19|NT_187693.1: 695,523-695,584 LILRP2
    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