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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
    nsv7099184copy number variation1nstd231human GRCh38.p12 chr1: 21,486,574-23,087,716 , GRCh37 chr1: 21,813,067-23,414,209 ALPL, C1QA, 36 more genes
    nsv7095949copy number variation1nstd102humanUncertain significance GRCh37 chr1: 19,199,339-24,690,861 , GRCh38.p12 chr1: 18,872,845-24,364,371 RPL29P6, NBPF3, 156 more genes
    nsv7095496copy number variation3nstd102humanUncertain significance GRCh37 chr1: 19,199,339-22,987,879 , GRCh38.p12 chr1: 18,872,845-22,661,386 RN7SL277P, MPHOSPH6P1, 103 more genes
    nsv7041020inversion1nstd229human GRCh38 chr1: 22,006,431-22,106,241 , GRCh37.p13 chr1: 22,332,924-22,432,734 CDC42, CELA3A, 6 more genes
    nsv6647365copy number variation1nstd229human GRCh38 chr1: 22,025,226-22,028,829 , GRCh37.p13 chr1: 22,351,719-22,355,322 LINC00339, LINC01635
    nsv6647357copy number variation1nstd229human GRCh38 chr1: 21,923,949-22,024,785 , GRCh37.p13 chr1: 22,250,442-22,351,278 RN7SL186P, LINC01635, 7 more genes
    nsv6647271copy number variation1nstd229human GRCh38 chr1: 22,020,386-22,035,158 , GRCh37.p13 chr1: 22,346,879-22,361,651 LINC00339, LINC01635, 1 more genes
    nsv6647254copy number variation1nstd229human GRCh38 chr1: 21,562,611-27,513,090 , GRCh37.p13 chr1: 21,889,104-27,839,601 RPL18AP5, LINC00339, 184 more genes
    nsv6647227copy number variation1nstd229human GRCh38 chr1: 20,848,934-27,947,465 , GRCh37.p13 chr1: 21,175,427-28,273,976 RPL17P9, ALPL, 218 more genes
    nsv6646744copy number variation1nstd229human GRCh38 chr1: 21,707,701-22,087,100 , GRCh37.p13 chr1: 22,034,194-22,413,593 LDLRAD2, HSPG2, 13 more genes
    nsv6626095copy number variation1nstd224human GRCh37 chr1: 22,345,093-22,373,624 , GRCh38.p12 chr1: 22,018,600-22,047,131 LINC00339, LINC01635, 1 more genes
    nsv6625979copy number variation1nstd224human GRCh37 chr1: 22,321,550-22,354,866 , GRCh38.p12 chr1: 21,995,057-22,028,373 LINC00339, LINC01635, 3 more genes
    nsv6334708copy number variation1nstd223human GRCh38 chr1: 22,019,801-22,022,500 , GRCh37.p13 chr1: 22,346,294-22,348,993 LINC01635
    nsv6326176copy number variation1nstd223human GRCh38 chr1: 22,014,349-22,033,433 , GRCh37.p13 chr1: 22,340,842-22,359,926 LINC00339, LINC01635, 1 more genes
    nsv6321594copy number variation1nstd223human GRCh38 chr1: 22,025,225-22,028,828 , GRCh37.p13 chr1: 22,351,718-22,355,321 LINC00339, LINC01635
    nsv6321020copy number variation1nstd223human GRCh38 chr1: 22,020,386-22,035,158 , GRCh37.p13 chr1: 22,346,879-22,361,651 LINC01635, CDC42-AS1, 1 more genes
    nsv6319052copy number variation1nstd223human GRCh38 chr1: 21,999,189-22,063,090 , GRCh37.p13 chr1: 22,325,682-22,389,583 CDC42, CELA3A, 5 more genes
    nsv6137724copy number variation1nstd102humanPathogenic GRCh37 chr1: 16,785,250-23,491,592 , GRCh38.p12 chr1: 16,458,755-23,165,099 PADI1, RPS15AP6, 176 more genes
    nsv6133948copy number variation1nstd213human GRCh37 chr1: 17,280,000-26,950,001 , GRCh38.p12 chr1: 16,953,505-26,623,510 ALPL, C1QA, 250 more genes
    nsv6133748copy number variation1nstd213human GRCh37 chr1: 17,270,000-26,960,001 , GRCh38.p12 chr1: 16,943,505-26,633,510 ALPL, C1QA, 250 more genes
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