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Items: 1 to 20 of 173

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5980461insertion1nstd102humanLikely benign GRCh37 chr10: 88,649,976-88,649,976 , GRCh38 chr10: 86,890,219-86,890,219 BMPR1A, RNU1-19P
    nsv5926561copy number variation1nstd209human GRCh38 chr10: 79,825,669-87,341,680 , GRCh37.p13 chr10: 81,585,425-89,101,437 , RPL12P29, 110 more genes
    nsv5672693copy number variation1nstd102humanPathogenic GRCh37 chr10: 88,598,623-88,659,889 , GRCh38.p12 chr10: 86,838,866-86,900,132 BMPR1A, RPAP2P1, 1 more genes
    nsv5380876copy number variation2nstd102humanUncertain significance GRCh37 chr10: 88,598,623-88,649,987 , GRCh38.p12 chr10: 86,838,866-86,890,230 BMPR1A, RPAP2P1, 1 more genes
    nsv5380793copy number variation1nstd102humanUncertain significance GRCh37 chr10: 88,603,164-88,651,992 , GRCh38.p12 chr10: 86,843,407-86,892,235 BMPR1A, RPAP2P1, 1 more genes
    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
    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
    nsv4728443copy number variation1nstd102humanPathogenic GRCh37 chr10: 88,598,737-88,649,818 , GRCh38.p12 chr10: 86,838,980-86,890,061 BMPR1A, RPAP2P1, 1 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
    nsv4682820copy number variation2nstd102humanUncertain significance GRCh37 chr10: 88,598,623-88,683,476 , GRCh38.p12 chr10: 86,838,866-86,923,719 BMPR1A, RPAP2P1, 1 more genes
    nsv4682267copy number variation4nstd102humanPathogenic, Uncertain significance GRCh37 chr10: 88,514,773-88,683,476 , GRCh38.p12 chr10: 86,755,016-86,923,719 RPAP2P1, RNU1-19P, 1 more genes
    nsv4681806copy number variation1nstd102humanUncertain significance GRCh37 chr10: 88,514,773-88,683,482 , GRCh38.p12 chr10: 86,755,016-86,923,725 RPAP2P1, BMPR1A, 1 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
    nsv4675794copy number variation1nstd102humanUncertain significance GRCh37 chr10: 88,586,190-88,708,342 , GRCh38.p12 chr10: 86,826,433-86,948,585 MMRN2, RNU1-19P, 2 more genes
    nsv4527772copy number variation1nstd166human GRCh37.p13 chr10: 88,582,999-88,708,500 , GRCh38.p12 chr10: 86,823,242-86,948,743 RPAP2P1, MMRN2, 2 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
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