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Items: 1 to 20 of 116

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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
    nsv6878478copy number variation1nstd229human GRCh38 chr10: 70,144,322-70,149,221 , GRCh37.p13 chr10: 71,904,078-71,908,977 TYSND1, SAR1A
    nsv6449936copy number variation1nstd223human GRCh38 chr10: 69,592,739-70,157,404 , GRCh37.p13 chr10: 71,352,495-71,917,160 RPL5P26, SAR1A, 12 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
    nsv6291213copy number variation1nstd102humanUncertain significance GRCh37 chr10: 71,754,361-72,399,690 , GRCh38.p12 chr10: 69,994,605-70,639,934 MACROH2A2, CEP57L1P1, 14 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
    nsv6095540insertion1nstd212human GRCh38 chr10: 70,147,137-70,147,137 , GRCh37.p13 chr10: 71,906,893-71,906,893 SAR1A, TYSND1
    nsv5492940copy number variation1nstd206human GRCh38 chr10: 70,137,367-70,137,424 , GRCh37.p13 chr10: 71,897,123-71,897,180 TYSND1
    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
    nsv4483835mobile element insertion1nstd166human GRCh37.p13 chr10: 71,897,744-71,897,744 , GRCh38.p12 chr10: 70,137,988-70,137,988 TYSND1
    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
    nsv4188936copy number variation1nstd166human GRCh37.p13 chr10: 71,897,123-71,897,180 , GRCh38.p12 chr10: 70,137,367-70,137,424 TYSND1
    nsv4187849copy number variation1nstd166human GRCh37.p13 chr10: 71,904,000-71,910,000 , GRCh38.p12 chr10: 70,144,244-70,150,244 TYSND1, SAR1A
    nsv4181465copy number variation1nstd166human GRCh37.p13 chr10: 71,841,888-71,923,766 , GRCh38.p12 chr10: 70,082,132-70,164,010 AIFM2, MACROH2A2, 3 more genes
    nsv4176020copy number variation1nstd166human GRCh37.p13 chr10: 71,901,013-71,901,681 , GRCh38.p12 chr10: 70,141,257-70,141,925 TYSND1
    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
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