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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095847copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr2: 108,604,612-109,579,739 , GRCh38.p12 chr2: 107,988,156-108,963,283 ACTP1, GCC2-AS1, 21 more genes
    nsv7046376inversion1nstd229human GRCh38 chr2: 106,214,512-108,776,331 , GRCh37.p13 chr2: 106,830,968-109,392,787 LOC107985931, LOC107985802, 42 more genes
    nsv7044675inversion1nstd229human GRCh38 chr2: 106,399,909-108,512,921 , GRCh37.p13 chr2: 107,016,365-109,129,377 GMCL1P2, SULT1C2, 30 more genes
    nsv7038094inversion1nstd229human GRCh38 chr2: 106,480,616-110,213,336 , GRCh37.p13 chr2: 107,097,072-110,970,913 WASF1P1, LOC105373985, 72 more genes
    nsv6693561copy number variation1nstd229human GRCh38 chr2: 108,167,602-108,293,652 , GRCh37.p13 chr2: 108,784,058-108,910,108 SETD6P1, LINC01594, 3 more genes
    nsv6690089copy number variation1nstd229human GRCh38 chr2: 108,253,924-108,297,536 , GRCh37.p13 chr2: 108,870,380-108,913,992 SULT1C3, WASF1P1, 1 more genes
    nsv6686700copy number variation1nstd229human GRCh38 chr2: 108,150,939-108,437,269 , GRCh37.p13 chr2: 108,767,395-109,053,725 SMIM12P1, SULT1C4, 8 more genes
    nsv6686545copy number variation1nstd229human GRCh38 chr2: 103,585,907-110,943,040 , GRCh37.p13 chr2: 104,202,365-111,700,617 PPP1R2P5, CAPZBP1, 142 more genes
    nsv6680242copy number variation1nstd229human GRCh38 chr2: 108,299,101-108,299,756 , GRCh37.p13 chr2: 108,915,557-108,916,212 SULT1C2
    nsv6634330copy number variation1nstd102humanPathogenic GRCh37 chr2: 11,504,318-111,365,996 , GRCh38.p12 chr2: 11,364,192-110,608,419 CYP1B1-AS1, LOC107985771, 1649 more genes
    nsv6627438copy number variation1nstd224human GRCh37 chr2: 108,921,033-108,968,224 , GRCh38.p12 chr2: 108,304,577-108,351,768 SULT1C5P, SULT1C2P2, 1 more genes
    nsv6627437copy number variation1nstd224human GRCh37 chr2: 108,816,885-108,970,321 , GRCh38.p12 chr2: 108,200,429-108,353,865 SULT1C2, SULT1C5P, 5 more genes
    nsv6348977copy number variation1nstd223human GRCh38 chr2: 108,300,579-108,366,973 , GRCh37.p13 chr2: 108,917,035-108,983,429 SULT1C5P, SULT1C2P2, 2 more genes
    nsv6348044copy number variation1nstd223human GRCh38 chr2: 107,883,785-108,500,628 , GRCh37.p13 chr2: 108,500,241-109,117,084 ACTP1, SLC5A7, 15 more genes
    nsv6315410copy number variation1nstd102humanUncertain significance GRCh37 chr2: 108,446,955-110,504,318 , GRCh38.p12 chr2: 107,830,499-109,746,741 SULT1C3, SH3RF3-AS1, 37 more genes
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6314726copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 40,607,042-146,902,764 , GRCh38.p12 chr2: 40,379,902-146,145,196 ACTG2, ACYP2, 1713 more genes
    nsv6313505copy number variation1nstd102humanPathogenic GRCh37 chr2: 108,446,955-110,504,318 , GRCh38.p12 chr2: 107,830,499-109,746,741 SULT1C3, SH3RF3-AS1, 37 more genes
    nsv6311333copy number variation1nstd102humanUncertain significance GRCh37 chr2: 108,604,612-109,378,671 , GRCh38.p12 chr2: 107,988,156-108,762,215 GMCL1P2, RPL10P5, 18 more genes
    nsv6290986copy number variation1nstd102humanLikely benign GRCh37 chr2: 108,534,031-109,132,283 , GRCh38.p12 chr2: 107,917,575-108,515,827 LINC01594, SRSF3P5, 14 more genes
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