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Items: 1 to 20 of 207

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7146716copy number variation1nstd232human GRCh37.p13 chr1: 220,990,858-220,990,921 , GRCh38.p12 chr1: 220,817,516-220,817,579 MTARC1
    nsv7099262copy number variation1nstd231human GRCh38.p12 chr1: 211,826,028-221,140,287 , GRCh37 chr1: 211,999,370-221,313,629 ATF3, CENPF, 114 more genes
    nsv7095972copy number variation1nstd102humanPathogenic GRCh37 chr1: 218,520,044-220,986,760 , GRCh38.p12 chr1: 218,346,702-220,813,418 TGFB2, LOC105373475, 38 more genes
    nsv7095587copy number variation1nstd102humanUncertain significance GRCh37 chr1: 220,088,791-220,986,760 , GRCh38.p12 chr1: 219,915,449-220,813,418 BPNT1, SNORA36B, 24 more genes
    nsv7052462inversion1nstd229human GRCh38 chr1: 219,653,745-221,511,784 , GRCh37.p13 chr1: 219,827,087-221,685,126 RNA5SP76, MIR215, 36 more genes
    nsv6677689copy number variation1nstd229human GRCh38 chr1: 220,789,074-220,789,138 , GRCh37.p13 chr1: 220,962,416-220,962,480 MTARC1
    nsv6677016copy number variation1nstd229human GRCh38 chr1: 220,797,545-220,797,904 , GRCh37.p13 chr1: 220,970,887-220,971,246 MTARC1
    nsv6666027copy number variation1nstd229human GRCh38 chr1: 220,746,301-220,790,400 , GRCh37.p13 chr1: 220,919,643-220,963,742 MTARC2, MTARC1
    nsv6665846copy number variation1nstd229human GRCh38 chr1: 220,723,171-220,788,956 , GRCh37.p13 chr1: 220,896,513-220,962,298 MTARC1, MTARC2
    nsv6664284copy number variation1nstd229human GRCh38 chr1: 220,813,618-220,813,720 , GRCh37.p13 chr1: 220,986,960-220,987,062 MTARC1
    nsv6663210copy number variation1nstd229human GRCh38 chr1: 220,817,516-220,817,580 , GRCh37.p13 chr1: 220,990,858-220,990,922 MTARC1
    nsv6662727copy number variation1nstd229human GRCh38 chr1: 220,781,273-220,787,434 , GRCh37.p13 chr1: 220,954,615-220,960,776 MTARC2, MTARC1
    nsv6661898copy number variation1nstd229human GRCh38 chr1: 220,757,404-220,848,174 , GRCh37.p13 chr1: 220,930,746-221,021,516 HLX-AS1, LINC01352, 3 more genes
    nsv6661132copy number variation1nstd229human GRCh38 chr1: 220,809,880-220,810,188 , GRCh37.p13 chr1: 220,983,222-220,983,530 MTARC1
    nsv6659296copy number variation1nstd229human GRCh38 chr1: 220,800,079-220,800,135 , GRCh37.p13 chr1: 220,973,421-220,973,477 MTARC1
    nsv6638068copy number variation1nstd102humanassociation GRCh38 chr1: 208,430,918-228,938,006 , GRCh37.p13 chr1: 208,604,263-229,073,753 AURKAP1, TLR5, 372 more genes
    nsv6634372copy number variation1nstd102humanPathogenic GRCh37 chr1: 197,867,914-249,224,684 , GRCh38.p12 chr1: 197,898,784-248,930,485 LOC105373279, YBX1P9, 1036 more genes
    nsv6540195inversion1nstd223human GRCh38 chr1: 216,397,966-226,054,144 , GRCh37.p13 chr1: 216,571,308-226,241,845 LOC105373046, CNIH3-AS1, 154 more genes
    nsv6321221copy number variation1nstd223human GRCh38 chr1: 220,787,701-220,788,500 , GRCh37.p13 chr1: 220,961,043-220,961,842 MTARC1
    nsv6320563copy number variation1nstd223human GRCh38 chr1: 220,817,516-220,817,580 , GRCh37.p13 chr1: 220,990,858-220,990,922 MTARC1
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