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Items: 1 to 20 of 107

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099232copy number variation1nstd231human GRCh38.p12 chr1: 151,364,317-152,231,192 , GRCh37 chr1: 151,336,793-152,203,668 , PSMB4, 37 more genes
    nsv7095245copy number variation1nstd102humanUncertain significance GRCh37 chr1: 151,801,885-152,287,932 , GRCh38.p12 chr1: 151,829,409-152,315,456 S100A10, C2CD4D, 18 more genes
    nsv7056666inversion1nstd229human GRCh38 chr1: 151,403,323-155,722,147 , GRCh37.p13 chr1: 151,375,799-155,691,938 ILF2, SPRR2C, 219 more genes
    nsv7056211inversion1nstd229human GRCh38 chr1: 143,881,700-152,159,818 , GRCh37.p13 chr1|NW_003871055.3: 697,113-7,283,150 , PDIA3P1, 333 more genes
    nsv7044458inversion1nstd229human GRCh38 chr1: 150,355,899-155,246,175 , GRCh37.p13 chr1: 150,440,214-155,215,966 LCE2C, MUC1, 254 more genes
    nsv7042502inversion1nstd229human GRCh38 chr1: 150,301,267-155,517,761 , GRCh37.p13 chr1: 150,440,214-155,487,552 LINGO4, CELF3, 268 more genes
    nsv6642170copy number variation1nstd229human GRCh38 chr1: 151,594,401-152,005,700 , GRCh37.p13 chr1: 151,566,877-151,978,176 CELF3, LINGO4, 17 more genes
    nsv6310678copy number variation4nstd102humanUncertain significance GRCh37 chr1: 149,895,434-156,851,434 , GRCh38.p12 chr1: 149,923,542-156,881,642 PRPF3, KHDC4, 352 more genes
    nsv6133734copy number variation1nstd213human GRCh37 chr1: 150,350,000-154,440,001 , GRCh38.p12 chr1: 150,377,524-154,467,525 , MCL1, 216 more genes
    nsv6133732copy number variation1nstd213human GRCh37 chr1: 149,750,000-153,310,001 , GRCh38.p12 chr1: 149,778,444-153,337,525 , CTSK, 183 more genes
    nsv6133555copy number variation1nstd213human GRCh37 chr1: 151,620,000-151,990,001 , GRCh38.p12 chr1: 151,647,524-152,017,525 RORC, THEM4, 18 more genes
    nsv6133499copy number variation1nstd213human GRCh37 chr1: 149,880,000-153,720,001 , GRCh38.p12 chr1: 149,908,448-153,747,525 , CTSK, 198 more genes
    nsv5381285copy number variation2nstd102humanUncertain significance GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699 , DCST1, 2428 more genes
    nsv4767860inversion1nstd199human GRCh37 chr1: 17,051,740-234,912,187 , GRCh38.p12 chr1: 16,725,245-234,776,440 , ABCA4, 4269 more genes
    nsv4751400inversion1nstd199human GRCh37 chr1: 17,125,657-234,919,132 , GRCh38.p12 chr1: 16,799,162-234,783,385 , ABCA4, 4264 more genes
    nsv4711935copy number variation1nstd195human GRCh37 chr1: 151,624,751-152,167,951 , GRCh38.p12 chr1: 151,652,275-152,195,475 , S100A11, 28 more genes
    nsv4674246copy number variation1nstd102humanUncertain significance GRCh37 chr1: 151,798,754-152,306,536 , GRCh38.p12 chr1: 151,826,278-152,334,060 LOC105371442, PUDPP2, 18 more genes
    nsv3963410insertion1nstd168human GRCh38 chr1: 151,833,450-151,852,411 , GRCh37.p13 chr1: 151,805,926-151,824,887 THEM5, C2CD4D-AS1, 1 more genes
    nsv3918947copy number variation1nstd102humanPathogenic NCBI36 chr1: 144,475,856-247,199,719 , GRCh37.p13 chr1: 145,764,499-249,233,096 , GRCh38.p12 chr1: 120,836,007-206,268,643 , LOC101060227, 1608 more genes
    nsv3912840copy number variation1nstd102humanPathogenic NCBI36 chr1: 144,764,751-247,199,719 , GRCh37.p13 chr1: 146,053,394-249,233,096 , GRCh38.p12 chr1: 120,836,007-206,268,643 , CRB1, 1608 more genes
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