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Items: 1 to 20 of 128

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098868copy number variation1nstd102humanPathogenic GRCh37 chr2: 121,981,917-122,363,471 , GRCh38.p12 chr2: 121,224,341-121,605,895 CLASP1, TFCP2L1, 3 more genes
    nsv7096196copy number variation1nstd102humanUncertain significance GRCh37 chr2: 121,684,917-122,288,605 , GRCh38.p12 chr2: 120,927,341-121,531,029 GLI2, RPS17P7, 6 more genes
    nsv7050777inversion1nstd229human GRCh38 chr2: 117,420,323-122,585,255 , GRCh37.p13 chr2: 118,177,899-123,342,831 LOC105373578, RPL17P15, 65 more genes
    nsv6696801copy number variation1nstd229human GRCh38 chr2: 120,749,236-121,378,541 , GRCh37.p13 chr2: 121,506,812-122,136,117 LOC105373587, RPS17P7, 4 more genes
    nsv6689134copy number variation1nstd229human GRCh38 chr2: 121,022,319-121,488,287 , GRCh37.p13 chr2: 121,779,895-122,245,863 LOC105373587, CLASP1, 3 more genes
    nsv6688404copy number variation1nstd229human GRCh38 chr2: 121,287,203-121,320,522 , GRCh37.p13 chr2: 122,044,779-122,078,098 RPS17P7
    nsv6637021copy number variation1nstd102humanPathogenic GRCh37 chr2: 121,241,775-126,487,783 , GRCh38.p12 chr2: 120,484,199-125,730,206 LOC105373590, LOC105373587, 32 more genes
    nsv6636871copy number variation1nstd102humanPathogenic GRCh37 chr2: 116,761,476-123,897,262 , GRCh38.p12 chr2: 116,003,900-123,139,686 LOC105373578, RPL17P15, 78 more genes
    nsv6553311inversion1nstd223human GRCh38 chr2: 113,382,126-121,687,299 , GRCh37.p13 chr2: 114,139,703-122,444,875 RPSAP23, CCDC93, 98 more genes
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6315168copy number variation1nstd102humanPathogenic GRCh37 chr2: 120,628,484-127,658,188 , GRCh38.p12 chr2: 119,870,908-126,900,612 TSN, LOC107985817, 58 more genes
    nsv6314748copy number variation1nstd102humanPathogenic GRCh37 chr2: 112,475,655-145,691,999 , GRCh38.p12 chr2: 111,718,078-144,934,432 MED15P9, TMEM37, 474 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
    nsv6313770copy number variation1nstd102humanPathogenic GRCh37 chr2: 113,188,197-128,144,700 , GRCh38.p12 chr2: 112,430,620-127,387,124 LOC105373575, RPS20P11, 174 more genes
    nsv6291353copy number variation1nstd102humanPathogenic GRCh37 chr2: 111,484,468-146,333,604 , GRCh38.p12 chr2: 110,726,891-145,576,036 LINC01120, LOC105373585, 490 more genes
    nsv6134420copy number variation1nstd213human GRCh37 chr2: 117,140,000-144,230,001 , GRCh38.p12 chr2: 116,382,424-143,472,432 BIN1, CCNT2, 382 more genes
    nsv6134239copy number variation1nstd213human GRCh37 chr2: 121,900,000-122,300,001 , GRCh38.p12 chr2: 121,142,424-121,542,425 CLASP1, TFCP2L1, 3 more genes
    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
    nsv5070275mobile element insertion1nstd203human GRCh38 chr2: 121,310,208-121,310,226 , GRCh37.p13 chr2: 122,067,784-122,067,802 RPS17P7
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