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Items: 1 to 20 of 145

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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
    nsv5039457inversion1nstd200human GRCh38 chr10: 84,138,634-84,960,031 , GRCh37.p13 chr10: 85,898,390-86,719,787 CCSER2, LRIT1, 14 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
    nsv4882543inversion1nstd200human GRCh37 chr10: 85,898,390-86,719,787 , GRCh38.p12 chr10: 84,138,634-84,960,031 LRIT2, CERNA2, 14 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
    nsv4679123copy number variation1nstd189human GRCh37.p13 chr10: 85,907,714-87,019,457 , GRCh38.p12 chr10: 84,147,958-85,259,701 RGR, LRIT1, 16 more genes
    nsv4528148copy number variation1nstd166human GRCh37.p13 chr10: 86,115,712-86,447,793 , GRCh38.p12 chr10: 84,355,956-84,688,037 RPS3AP5, CACYBPP1, 3 more genes
    nsv4456337copy number variation1nstd102humanUncertain significance GRCh37 chr10: 85,030,876-86,392,391 , GRCh38.p12 chr10: 83,271,120-84,632,635 RNU6-129P, HMGN2P8, 22 more genes
    nsv4349613copy number variation1nstd102humanPathogenic GRCh37 chr10: 81,697,811-88,768,847 , GRCh38.p12 chr10: 79,938,055-87,009,090 MIR346, LOC101929662, 91 more genes
    nsv4343722sequence alteration1nstd166human GRCh37.p13 chr10: 43,905,894-92,001,956 , GRCh38.p12 chr10: 43,410,446-90,242,199 , ALOX5, 749 more genes
    nsv4339713sequence alteration1nstd166human GRCh37.p13 chr10: 8,718,069-114,609,729 , GRCh38.p12 chr10: 8,676,106-112,849,970 , ADRA2A, 1651 more genes
    nsv4329567inversion1nstd166human GRCh37.p13 chr10: 78,733,163-90,441,950 , GRCh38.p12 chr10: 76,973,405-88,682,193 , ANXA11, 187 more genes
    nsv3924859copy number variation1nstd102humanPathogenic NCBI36 chr10: 52,159,133-88,896,941 , GRCh38 chr10: 50,729,367-87,147,204 , GRCh37 chr10: 52,489,127-88,906,961 BMS1P4-AGAP5, MTCO2P23, 471 more genes
    nsv3923084copy number variation1nstd102humanPathogenic NCBI36 chr10: 81,149,191-89,108,131 , GRCh38 chr10: 79,719,429-87,358,394 , GRCh37 chr10: 81,479,185-89,118,151 LINC02650, GHITM, 110 more genes
    nsv3922892copy number variation1nstd102humanPathogenic GRCh38 chr10: 79,802,022-87,068,261 , GRCh37 chr10: 81,561,459-88,828,018 , NCBI36 chr10: 81,263,385-88,817,998 LINC02655, LOC105378409, 103 more genes
    nsv3922465copy number variation1nstd102humanPathogenic GRCh37 chr10: 81,658,272-88,869,584 , GRCh38 chr10: 79,898,516-87,109,827 , NCBI36 chr10: 81,648,252-88,859,564 FARSBP1, ADIRF, 97 more genes
    nsv3920295copy number variation1nstd102humanPathogenic NCBI36 chr10: 81,675,342-135,374,737 , GRCh37.p13 chr10: 81,685,362-135,524,747 , GRCh38.p12 chr10: 79,925,606-133,787,422 EIF2S2P3, CYP17A1-AS1, 895 more genes
    nsv3920201copy number variation1nstd102humanUncertain significance NCBI36 chr10: 85,053,536-86,738,788 , GRCh38 chr10: 83,303,800-84,989,052 , GRCh37 chr10: 85,063,556-86,748,808 LOC105378393, LRIT1, 25 more genes
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