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Items: 1 to 20 of 176

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5919342copy number variation1nstd209human GRCh38 chr8: 72,905,491-79,590,734 , GRCh37.p13 chr8: 73,817,726-80,502,969 , GYG1P1, 73 more genes
    nsv5364245translocation1nstd200human GRCh38 chrX: 100,838,935-100,838,935 , GRCh38 chr8: 73,945,612-73,945,612 , GRCh37.p13 chrX: 100,093,924-100,093,924 , GRCh37.p13 chr8: 74,857,847-74,857,847 ELOC, CSTF2
    nsv5332432translocation1nstd200human GRCh37 chrX: 100,093,924-100,093,924 , GRCh37 chr8: 74,857,847-74,857,847 , GRCh38.p12 chrX: 100,838,935-100,838,935 , GRCh38.p12 chr8: 73,945,612-73,945,612 ELOC, CSTF2
    nsv5312589copy number variation1nstd204human GRCh38.p13 chr8: 73,954,985-73,955,301 , GRCh37.p13 chr8: 74,867,220-74,867,536 ELOC
    nsv5036483inversion1nstd200human GRCh38 chr8: 71,454,844-121,935,245 , GRCh37.p13 chr8: 72,367,079-122,947,484 , LINC01617, 636 more genes
    nsv4960953copy number variation1nstd200human GRCh38 chr8: 73,964,015-73,968,923 , GRCh37.p13 chr8: 74,876,250-74,881,158 ELOC
    nsv4821990copy number variation1nstd200human GRCh37 chr8: 74,876,250-74,881,158 , GRCh38.p12 chr8: 73,964,015-73,968,923 ELOC
    nsv4456811copy number variation1nstd102humanPathogenic GRCh37 chr8: 31,936,551-146,295,771 , GRCh38.p12 chr8: 32,079,035-145,070,385 TERF1, LOC107986945, 1511 more genes
    nsv4349554copy number variation2nstd102humanPathogenic GRCh37 chr8: 158,048-146,295,771 , GRCh38.p12 chr8: 208,048-145,070,385 LOC101929488, TEX15, 2105 more genes
    nsv4332062inversion1nstd166human GRCh37.p13 chr8: 70,438,609-99,073,700 , GRCh38.p12 chr8: 69,526,374-98,061,472 , FTH1P11, 375 more genes
    nsv4318272inversion1nstd166human GRCh37.p13 chr8: 51,271,211-76,167,888 , GRCh38.p12 chr8: 50,358,651-75,255,653 , ASPH, 341 more genes
    nsv4158779copy number variation1nstd166human GRCh37.p13 chr8: 74,876,250-74,881,158 , GRCh38.p12 chr8: 73,964,015-73,968,923 ELOC
    nsv3923310copy number variation1nstd102humanPathogenic NCBI36 chr8: 166,452-146,264,902 , GRCh38 chr8: 226,452-145,068,712 , GRCh37 chr8: 176,452-146,294,098 LOC112268023, RPL23AP96, 2105 more genes
    nsv3923011copy number variation1nstd102humanPathogenic GRCh38 chr8: 66,171,669-93,505,509 , GRCh37 chr8: 67,083,904-94,517,737 , NCBI36 chr8: 67,246,458-94,586,913 CA3, HAUS1P3, 353 more genes
    nsv3922848copy number variation1nstd102humanPathogenic NCBI36 chr8: 74,954,174-86,710,947 , GRCh37 chr8: 74,791,620-86,523,695 , GRCh38 chr8: 73,879,385-85,611,466 MITA1, CA3-AS1, 139 more genes
    nsv3922631copy number variation1nstd102humanPathogenic GRCh38 chr8: 61,691,800-82,537,696 , NCBI36 chr8: 62,766,913-83,612,486 , GRCh37 chr8: 62,604,359-83,449,931 NCOA2, LOC107986893, 284 more genes
    nsv3922586copy number variation1nstd102humanUncertain significance GRCh37 chr8: 74,874,590-75,661,695 , NCBI36 chr8: 75,037,144-75,824,250 , GRCh38 chr8: 73,962,355-74,749,460 TMEM70, MIR5681B, 15 more genes
    nsv3919282copy number variation1nstd102humanPathogenic GRCh37 chr8: 191,530-146,280,020 , GRCh38 chr8: 241,530-145,054,634 , NCBI36 chr8: 181,530-146,250,824 MIR4662B, LOC101927845, 2104 more genes
    nsv3919200copy number variation1nstd102humanPathogenic GRCh38 chr8: 241,530-145,049,449 , GRCh37 chr8: 191,530-146,274,835 , NCBI36 chr8: 181,530-146,245,639 LOC112268023, LOC105375925, 2103 more genes
    nsv3918934copy number variation1nstd102humanPathogenic GRCh37 chr8: 71,860,628-75,265,519 , NCBI36 chr8: 72,023,182-75,428,074 , GRCh38 chr8: 70,948,393-74,353,284 XKR9, C8orf89, 47 more genes
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