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Items: 1 to 20 of 165

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137211copy number variation1nstd102humanPathogenic GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639 EXOC6, VCL, 1906 more genes
    nsv7137209copy number variation1nstd102humanPathogenic GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639 RNU7-12P, RNU1-65P, 1876 more genes
    nsv6891469copy number variation1nstd229human GRCh38 chr10: 69,206,774-69,212,570 , GRCh37.p13 chr10: 70,966,530-70,972,326 SUPV3L1
    nsv6884395copy number variation1nstd229human GRCh38 chr10: 69,063,514-69,243,293 , GRCh37.p13 chr10: 70,823,270-71,003,049 SUPV3L1, LOC101928994, 4 more genes
    nsv6579902inversion1nstd223human GRCh38 chr10: 69,184,323-69,185,742 , GRCh37.p13 chr10: 70,944,079-70,945,498 SUPV3L1
    nsv6314185copy number variation1nstd102humanPathogenic GRCh37 chr10: 68,735,254-78,885,714 , GRCh38.p12 chr10: 66,975,496-77,125,956 SLC25A16, CTNNA3, 204 more genes
    nsv6308916copy number variation1nstd102humanUncertain significance GRCh37 chr10: 67,680,088-71,332,799 , GRCh38.p12 chr10: 65,920,330-69,573,043 RPS3AP38, MIR7151, 62 more genes
    nsv6278792insertion1nstd214human GRCh38 chr10: 69,194,754-69,194,754 , GRCh37.p13 chr10: 70,954,510-70,954,510 SUPV3L1
    nsv6143934copy number variation1nstd206human GRCh38 chr10: 69,194,754-69,194,824 , GRCh37.p13 chr10: 70,954,510-70,954,580 SUPV3L1
    nsv6131969copy number variation1nstd213human GRCh37 chr10: 70,900,000-71,490,001 , GRCh38.p12 chr10: 69,140,244-69,730,245 SUPV3L1, MTND1P20, 19 more genes
    nsv5631548insertion1nstd207human GRCh38 chr10: 69,194,754-69,194,754 , GRCh37.p13 chr10: 70,954,510-70,954,510 SUPV3L1
    nsv5030933inversion1nstd200human GRCh38 chr10: 57,233,666-95,028,660 , GRCh37.p13 chr10: 58,993,426-96,788,417 , RNU6-740P, 615 more genes
    nsv4647954copy number variation1nstd186human GRCh37 chr10: 70,954,510-70,954,580 , GRCh38.p12 chr10: 69,194,754-69,194,824 SUPV3L1
    nsv4601421copy number variation1nstd183human GRCh37 chr10: 70,564,120-74,122,461 , GRCh38.p12 chr10: 68,804,363-72,362,703 , SGPL1, 79 more genes
    nsv4528649copy number variation1nstd166human GRCh37.p13 chr10: 70,954,510-70,954,580 , GRCh38.p12 chr10: 69,194,754-69,194,824 SUPV3L1
    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
    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
    nsv3922335copy number variation1nstd102humanPathogenic GRCh37 chr10: 60,196,226-76,174,974 , GRCh38 chr10: 58,436,466-74,415,216 , NCBI36 chr10: 59,866,232-75,844,980 UNC5B-AS1, ALDH7A1P4, 250 more genes
    nsv3917966copy number variation1nstd102humanPathogenic NCBI36 chr10: 68,626,331-80,851,819 , GRCh37 chr10: 68,956,325-81,181,813 , GRCh38 chr10: 67,196,567-79,422,057 LINC02640, HK1, 231 more genes
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