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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7052468inversion1nstd229human GRCh38 chr2: 109,726,921-110,637,321 , GRCh37.p13 chr2: 110,484,498-111,394,898 LOC105373553, NPHP1, 39 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
    nsv6634363copy number variation1nstd102humanUncertain significance GRCh37 chr2: 110,498,141-111,365,996 , GRCh38.p12 chr2: 109,740,564-110,608,419 NPHP1, MIR4436B1, 34 more genes
    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
    nsv6315445copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr2: 110,504,318-111,365,996 , GRCh38.p12 chr2: 109,746,741-110,608,419 LOC107985776, LOC105375809, 34 more genes
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6314776copy number variation1nstd220human GRCh37 chr2: 111,195,659-113,121,587 , GRCh38.p12 chr2: 110,438,082-112,364,010 BUB1, BCL2L11, 35 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
    nsv6296859copy number variation1nstd186human GRCh37 chr2: 111,153,195-111,159,577 , GRCh38.p12 chr2: 110,395,618-110,402,000 LOC100288570, LIMS4
    nsv6140183copy number variation1nstd206human GRCh38 chr2: 110,421,618-110,427,618 , GRCh37.p13 chr2: 111,179,195-111,185,195 LIMS4, LOC100288570
    nsv6140172copy number variation1nstd206human GRCh38 chr2: 110,394,904-110,441,050 , GRCh37.p13 chr2: 111,152,481-111,198,627 LOC100288570, LIMS4
    nsv6139797copy number variation1nstd206human GRCh38 chr2: 110,395,618-110,412,000 , GRCh37.p13 chr2: 111,153,195-111,169,577 LOC100288570, LIMS4
    nsv6139757copy number variation1nstd206human GRCh38 chr2: 110,395,618-110,402,000 , GRCh37.p13 chr2: 111,153,195-111,159,577 LIMS4, LOC100288570
    nsv6139401copy number variation1nstd206human GRCh38 chr2: 110,321,784-110,415,118 , GRCh37.p13 chr2: 111,079,361-111,172,695 LINC01106, LOC442041, 7 more genes
    nsv5985309copy number variation1nstd212human GRCh38 chr2: 108,715,210-112,293,808 , GRCh37.p13 chr2: 109,331,666-113,051,385 , NPHP1, 85 more genes
    nsv5567265copy number variation1nstd207human GRCh38 chr2: 110,440,965-110,441,263 , GRCh37.p13 chr2: 111,198,542-111,198,840 LIMS4
    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
    nsv5442426copy number variation1nstd206human GRCh38 chr2: 109,913,618-110,441,618 , GRCh37.p13 chr2: 110,671,195-111,199,195 LIMS3-LOC440895, LOC105373547, 28 more genes
    nsv5435652copy number variation1nstd206human GRCh38 chr2: 110,323,618-110,440,200 , GRCh37.p13 chr2: 111,081,195-111,197,777 LINC01106, LOC442041, 7 more genes
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