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Items: 1 to 20 of 193

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7046376inversion1nstd229human GRCh38 chr2: 106,214,512-108,776,331 , GRCh37.p13 chr2: 106,830,968-109,392,787 LOC107985931, LOC107985802, 42 more genes
    nsv6692711copy number variation1nstd229human GRCh38 chr2: 106,190,823-106,671,141 , GRCh37.p13 chr2: 106,807,279-107,287,597 RPL27AP4, RPL22P10, 9 more genes
    nsv6687902copy number variation1nstd229human GRCh38 chr2: 106,312,436-106,402,214 , GRCh37.p13 chr2: 106,928,892-107,018,670 ILRUNP1, PLGLA, 2 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
    nsv6685124copy number variation1nstd229human GRCh38 chr2: 106,174,659-106,809,550 , GRCh37.p13 chr2: 106,791,115-107,426,006 PLGLA, UXS1, 12 more genes
    nsv6680663copy number variation1nstd229human GRCh38 chr2: 106,371,462-106,384,640 , GRCh37.p13 chr2: 106,987,918-107,001,096 PLGLA, ANAPC1P6
    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
    nsv6627304copy number variation1nstd224human GRCh37 chr2: 106,886,935-108,440,138 , GRCh38.p12 chr2: 106,270,479-107,823,682 EEF1A1P12, ILRUNP1, 17 more genes
    nsv6346431copy number variation1nstd223human GRCh38 chr2: 106,312,436-106,402,214 , GRCh37.p13 chr2: 106,928,892-107,018,670 PLGLA, ANAPC1P6, 2 more genes
    nsv6342583copy number variation1nstd223human GRCh38 chr2: 106,174,659-106,809,550 , GRCh37.p13 chr2: 106,791,115-107,426,006 ILRUNP1, RPS21P2, 12 more genes
    nsv6337069copy number variation1nstd223human GRCh38 chr2: 106,239,641-107,907,583 , GRCh37.p13 chr2: 106,856,097-108,524,039 ST6GAL2, ILRUNP1, 20 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
    nsv6298334copy number variation1nstd186human GRCh37 chr2: 106,895,533-107,134,207 , GRCh38.p12 chr2: 106,279,077-106,517,751 , CD8B2, 7 more genes
    nsv6291269copy number variation1nstd102humanLikely benign GRCh37 chr2: 106,872,677-108,440,756 , GRCh38.p12 chr2: 106,256,221-107,824,300 LOC105373539, RPS21P2, 17 more genes
    nsv6291220copy number variation1nstd102humanUncertain significance GRCh37 chr2: 106,791,212-107,425,876 , GRCh38.p12 chr2: 106,174,756-106,809,420 PLGLA, EEF1A1P12, 12 more genes
    nsv5868662copy number variation1nstd209human GRCh38 chr2: 106,240,685-107,908,171 , GRCh37.p13 chr2: 106,857,141-108,524,627 , LOC105373539, 21 more genes
    nsv5565143copy number variation1nstd207human GRCh38 chr2: 106,388,991-106,389,042 , GRCh37.p13 chr2: 107,005,447-107,005,498 PLGLA
    nsv5558142mobile element insertion1nstd206human GRCh38 chr2: 102,295,972-141,288,199 , GRCh37.p13 chr2: 102,912,432-142,045,768 , LOC105373587, 623 more genes
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
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