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Items: 1 to 20 of 144

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5978109inversion1nstd209human GRCh38 chr19: 54,222,352-54,696,988 , GRCh37.p13 chr19|NW_004166865.1: 196,719-671,355 LAIR1, LAIR2, 29 more genes
    nsv5941514copy number variation1nstd209human GRCh38 chr19: 54,505,233-54,507,683 , GRCh37.p13 chr19|NW_004166865.1: 479,600-482,050 LAIR2
    nsv5873504copy number variation1nstd209human GRCh38 chr19: 54,505,206-54,507,734 , GRCh37.p13 chr19|NW_004166865.1: 479,573-482,101 LAIR2
    nsv5562753sequence alteration1nstd206human GRCh38 chr19: 54,280,539-54,594,201 , GRCh37.p13 chr19|NW_004166865.1: 254,906-568,568 LAIR1, LILRB2, 16 more genes
    nsv5530582copy number variation1nstd206human GRCh38 chr19: 54,505,235-54,507,684 , GRCh37.p13 chr19|NW_004166865.1: 479,602-482,051 LAIR2
    nsv5322945copy number variation1nstd204human GRCh38.p13 chr19: 54,505,204-54,507,715 , GRCh37.p13 chr19|NW_004166865.1: 479,571-482,082 LAIR2
    nsv5296629copy number variation1nstd204human GRCh38.p13 chr19: 54,505,201-54,507,700 , GRCh37.p13 chr19|NW_004166865.1: 479,568-482,067 LAIR2
    nsv5285996copy number variation1nstd204human GRCh38.p13 chr19: 54,505,206-54,507,734 , GRCh37.p13 chr19|NW_004166865.1: 479,573-482,101 LAIR2
    nsv5028025copy number variation1nstd200human GRCh38 chr19: 54,501,385-54,503,196 , GRCh37.p13 chr19|NW_004166865.1: 475,752-477,563 LAIR2
    nsv5024937copy number variation1nstd200human GRCh38 chr19: 54,476,380-54,552,177 , GRCh37.p13 chr19|NW_004166865.1: 450,747-526,544 LAIR2, KIR3DX1, 1 more genes
    nsv4865327copy number variation1nstd200human GRCh37 chr19: 54,953,581-55,047,420 , GRCh38.p12 chr19: 54,442,399-54,536,201 , GRCh38.p12 chr19|NT_187693.1: 424,695-518,534 , GRCh38.p12 chr19|NW_003571060.1: 347,089-440,928 , GRCh38.p12 chr19|NW_003571054.1: 348,915-442,411 KIR3DX1, LENG8-AS1, 5 more genes
    nsv4861352copy number variation1nstd200human GRCh37 chr19: 55,016,451-55,018,899 , GRCh38.p12 chr19|NT_187693.1: 487,565-490,013 , GRCh38.p12 chr19|NW_003571060.1: 409,952-412,402 , GRCh38.p12 chr19|NW_003571054.1: 411,442-413,890 , GRCh38.p12 chr19: 54,505,235-54,507,684 LAIR2
    nsv4861346copy number variation1nstd200human GRCh37 chr19: 54,836,186-55,143,468 , GRCh38.p12 chr19|NT_187693.1: 307,300-614,582 , GRCh38.p12 chr19|NW_003571060.1: 258,364-536,895 , GRCh38.p12 chr19|NW_003571054.1: 306,331-538,403 , GRCh38.p12 chr19: 54,324,914-54,632,017 LAIR2, LILRA4, 14 more genes
    nsv4760099inversion1nstd199human GRCh37 chr19: 54,786,152-55,139,147 , GRCh38.p12 chr19: 54,282,297-54,627,696 , GRCh38.p12 chr19|NT_187693.1: 257,266-610,261 , GRCh38.p12 chr19|NW_003571060.1: 258,364-532,574 , GRCh38.p12 chr19|NW_003571054.1: 257,036-534,082 LAIR1, LAIR2, 18 more genes
    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
    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
    nsv4676308copy number variation1nstd102humanLikely benign GRCh37 chr19: 55,017,885-55,157,759 , GRCh38.p12 chr19|NW_003571054.1: 412,876-552,694 , GRCh38.p12 chr19|NT_187693.1: 488,999-628,873 , GRCh38.p12 chr19|NW_003571060.1: 411,387-551,189 , GRCh38.p12 chr19: 54,506,669-54,646,310 LOC105372461, LAIR2, 8 more genes
    nsv4559571sequence alteration1nstd166human GRCh37.p13 chr19: 54,801,097-55,088,154 , GRCh38.p12 chr19|NT_187693.1: 272,211-559,268 , GRCh38.p12 chr19|NW_003571060.1: 258,364-481,571 , GRCh38.p12 chr19|NW_003571054.1: 271,982-483,077 , GRCh38.p12 chr19: 54,297,011-54,576,687 LILRA4, CDC42EP5, 15 more genes
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