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Items: 1 to 20 of 183

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5963863insertion1nstd209human GRCh38 chr10: 114,246,525-114,246,525 , GRCh37.p13 chr10: 116,006,284-116,006,284 AURKAP2, VWA2
    nsv5699599mobile element insertion1nstd211human GRCh38 chr10: 114,253,419-114,253,419 , GRCh37.p13 chr10: 116,013,178-116,013,178 VWA2
    nsv5694809mobile element insertion2nstd211human GRCh38 chr10: 114,244,642-114,244,642 , GRCh37.p13 chr10: 116,004,401-116,004,401 VWA2, AURKAP2
    nsv5639231insertion1nstd207human GRCh38 chr10: 114,253,198-114,253,198 , GRCh37.p13 chr10: 116,012,957-116,012,957 VWA2
    nsv5327857inversion1nstd204human GRCh37.p13 chr10: 115,288,018-116,786,304 , GRCh38.p13 chr10: 113,528,259-115,723,405 , ADRB1, 31 more genes
    nsv5029881inversion1nstd200human GRCh38 chr10: 113,528,269-115,723,396 , GRCh37.p13 chr10: 115,288,028-116,786,295 , NHLRC2, 31 more genes
    nsv4977043copy number variation1nstd200human GRCh38 chr10: 114,263,514-114,267,562 , GRCh37.p13 chr10: 116,023,273-116,027,321 VWA2
    nsv4977042copy number variation1nstd200human GRCh38 chr10: 114,247,506-114,252,760 , GRCh37.p13 chr10: 116,007,265-116,012,519 AURKAP2, VWA2
    nsv4977041copy number variation1nstd200human GRCh38 chr10: 114,246,185-114,246,793 , GRCh37.p13 chr10: 116,005,944-116,006,552 VWA2, AURKAP2
    nsv4880587inversion1nstd200human GRCh37 chr10: 115,288,028-117,482,906 , GRCh38.p12 chr10: 113,528,269-115,723,396 , NHLRC2, 31 more genes
    nsv4755988insertion1nstd199human GRCh37 chr10: 116,012,941-116,012,941 , GRCh38.p12 chr10: 114,253,182-114,253,182 VWA2
    nsv4538027insertion1nstd166human GRCh37.p13 chr10: 116,015,929-116,015,929 , GRCh38.p12 chr10: 114,256,170-114,256,170 VWA2
    nsv4456626copy number variation1nstd102humanPathogenic GRCh37 chr10: 114,544,537-135,427,143 , GRCh38.p12 chr10: 112,784,778-133,613,639 LOC105378521, ZRANB1, 317 more genes
    nsv4444116insertion1nstd175human GRCh37 chr10: 116,012,942-116,012,942 , GRCh38.p12 chr10: 114,253,183-114,253,183 VWA2
    nsv4348764copy number variation1nstd102humanPathogenic GRCh37 chr10: 110,022,170-135,439,095 , GRCh38.p12 chr10: 108,262,412-133,625,591 LOC105378492, VENTX, 373 more genes
    nsv4188483copy number variation1nstd166human GRCh37.p13 chr10: 116,009,707-116,013,629 , GRCh38.p12 chr10: 114,249,948-114,253,870 VWA2
    nsv4184002copy number variation1nstd166human GRCh37.p13 chr10: 116,033,373-116,037,400 , GRCh38.p12 chr10: 114,273,614-114,277,641 VWA2
    nsv4183836copy number variation1nstd166human GRCh37.p13 chr10: 116,046,459-116,046,542 , GRCh38.p12 chr10: 114,286,700-114,286,783 VWA2, AFAP1L2
    nsv4183720copy number variation1nstd166human GRCh37.p13 chr10: 116,030,341-117,443,667 , GRCh38.p12 chr10: 114,270,582-115,684,157 VWA2, AFAP1L2, 14 more genes
    nsv3960347insertion1nstd168human GRCh38 chr10: 114,239,781-114,243,729 , GRCh37.p13 chr10: 115,999,540-116,003,488 VWA2
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