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Items: 1 to 20 of 231

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5926561copy number variation1nstd209human GRCh38 chr10: 79,825,669-87,341,680 , GRCh37.p13 chr10: 81,585,425-89,101,437 , RPL12P29, 110 more genes
    nsv5672610copy number variation1nstd102humanPathogenic GRCh37 chr10: 88,683,123-89,725,321 , GRCh38.p12 chr10: 86,923,366-87,965,564 FAM245A, BMPR1A, 30 more genes
    nsv5365019translocation1nstd200human GRCh38 chr10: 86,959,942-86,959,942 , GRCh38 chr10: 86,962,935-86,962,935 , GRCh37.p13 chr10: 88,722,692-88,722,692 , GRCh37.p13 chr10: 88,719,699-88,719,699 SNCG, MMRN2
    nsv5365018translocation1nstd200human GRCh38 chr10: 86,960,250-86,960,250 , GRCh38 chr10: 86,959,912-86,959,912 , GRCh37.p13 chr10: 88,720,007-88,720,007 , GRCh37.p13 chr10: 88,719,669-88,719,669 SNCG, MMRN2
    nsv5341528translocation1nstd200human GRCh37 chr10: 88,719,699-88,719,699 , GRCh37 chr10: 88,722,692-88,722,692 , GRCh38.p12 chr10: 86,959,942-86,959,942 , GRCh38.p12 chr10: 86,962,935-86,962,935 MMRN2, SNCG
    nsv5336826translocation1nstd200human GRCh37 chr10: 88,719,669-88,719,669 , GRCh37 chr10: 88,720,007-88,720,007 , GRCh38.p12 chr10: 86,959,912-86,959,912 , GRCh38.p12 chr10: 86,960,250-86,960,250 SNCG, MMRN2
    nsv5308226copy number variation1nstd204human GRCh37.p13 chr10: 88,714,467-88,714,768 , GRCh38.p13 chr10: 86,954,710-86,955,011 MMRN2, SNCG
    nsv5251529copy number variation1nstd204human GRCh38.p13 chr10: 86,954,201-86,963,800 , GRCh37.p13 chr10: 88,713,958-88,723,557 MMRN2, SNCG
    nsv5036801inversion1nstd200human GRCh38 chr10: 86,632,260-87,196,230 , GRCh37.p13 chr10: 88,392,017-88,955,987 SHLD2, BMPR1A, 15 more genes
    nsv5030933inversion1nstd200human GRCh38 chr10: 57,233,666-95,028,660 , GRCh37.p13 chr10: 58,993,426-96,788,417 , RNU6-740P, 615 more genes
    nsv4875742inversion1nstd200human GRCh37 chr10: 88,392,017-88,955,987 , GRCh38.p12 chr10: 86,632,260-87,196,230 LOC105378410, LDB3, 15 more genes
    nsv4729624copy number variation1nstd102humanPathogenic GRCh37 chr10: 88,685,387-92,144,296 , GRCh38.p12 chr10: 86,925,630-90,384,539 LOC105378414, RN7SL78P, 84 more genes
    nsv4729484copy number variation1nstd102humanPathogenic GRCh37 chr10: 81,457,752-89,253,430 , GRCh38.p12 chr10: 79,697,996-87,493,673 DPY19L2P5, TSPAN14-AS1, 115 more genes
    nsv4729317copy number variation1nstd102humanPathogenic GRCh37 chr10: 81,617,260-89,146,780 , GRCh38.p12 chr10: 79,857,504-87,387,023 LOC105378390, LRIT1, 109 more genes
    nsv4728260copy number variation1nstd102humanPathogenic GRCh37 chr10: 81,585,301-89,101,700 , GRCh38.p12 chr10: 79,825,545-87,341,943 C1DP3, RNA5SP322, 109 more genes
    nsv4683124copy number variation2nstd102humanPathogenic GRCh37 chr10: 88,514,773-89,725,321 , GRCh38.p12 chr10: 86,755,016-87,965,564 NUTM2A, RPS26P38, 32 more genes
    nsv4681457copy number variation1nstd102humanPathogenic GRCh37 chr10: 88,428,449-88,713,917 , GRCh38.p12 chr10: 86,668,692-86,954,160 BMPR1A, SNCG, 4 more genes
    nsv4454138copy number variation1nstd102humanPathogenic GRCh38 chr10: 86,755,016-87,965,482 , GRCh37 chr10: 88,514,773-89,725,239 PAPSS2, KLLN, 32 more genes
    nsv4453333copy number variation1nstd102humanPathogenic GRCh37 chr10: 88,598,623-89,725,239 , GRCh38 chr10: 86,838,866-87,965,482 PTEN, BMS1P3, 32 more genes
    nsv4450849copy number variation1nstd102humanPathogenic GRCh38 chr10: 86,875,868-87,894,129 , GRCh37 chr10: 88,635,625-89,653,886 NUTM2D, ADIRF, 30 more genes
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