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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
    nsv7093887copy number variation1nstd102humanUncertain significance GRCh37 chr10: 72,576,610-72,648,290 , GRCh38.p12 chr10: 70,816,854-70,888,533 SGPL1, PCBD1
    nsv6892303copy number variation1nstd229human GRCh38 chr10: 70,836,234-70,989,811 , GRCh37.p13 chr10: 72,595,991-72,749,568 LINC02622, PCBD1, 2 more genes
    nsv6882612copy number variation1nstd229human GRCh38 chr10: 70,881,215-70,881,611 , GRCh37.p13 chr10: 72,640,972-72,641,368 PCBD1, SGPL1
    nsv6620675copy number variation1nstd224human GRCh37 chr10: 72,012,813-73,062,048 , GRCh38.p12 chr10: 70,253,057-71,302,291 ADAMTS14, TBATA, 17 more genes
    nsv6620606copy number variation1nstd224human GRCh37 chr10: 72,109,893-72,996,234 , GRCh38.p12 chr10: 70,350,137-71,236,477 NODAL, PCBD1, 15 more genes
    nsv6444872copy number variation1nstd223human GRCh38 chr10: 70,293,423-70,921,060 , GRCh37.p13 chr10: 72,053,179-72,680,817 PALD1, YY1P1, 10 more genes
    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
    nsv6131888copy number variation1nstd213human GRCh37 chr10: 71,890,000-72,730,001 , GRCh38.p12 chr10: 70,130,244-70,970,244 NPFFR1, TBATA, 18 more genes
    nsv5713734mobile element insertion2nstd211human GRCh38 chr10: 70,885,972-70,885,972 , GRCh37.p13 chr10: 72,645,729-72,645,729 PCBD1
    nsv5399922mobile element insertion1nstd206human GRCh38 chr10: 70,885,972-70,886,023 , GRCh37.p13 chr10: 72,645,729-72,645,780 PCBD1
    nsv5030933inversion1nstd200human GRCh38 chr10: 57,233,666-95,028,660 , GRCh37.p13 chr10: 58,993,426-96,788,417 , RNU6-740P, 615 more genes
    nsv4601421copy number variation1nstd183human GRCh37 chr10: 70,564,120-74,122,461 , GRCh38.p12 chr10: 68,804,363-72,362,703 , SGPL1, 79 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
    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
    nsv3924153copy number variation1nstd102humanUncertain significance NCBI36 chr10: 72,026,140-72,717,991 , GRCh38 chr10: 70,596,378-71,288,228 , GRCh37 chr10: 72,356,134-73,047,985 LOC105378351, ADAMTS14, 10 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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