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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3893786copy number variation1nstd102humanPathogenic GRCh37.p13 chrX|NW_004070890.2: 3,458,159-3,475,397 , NCBI36 chrX: 146,822,978-146,840,216 , GRCh38 chrX: 147,933,767-147,951,004 FMR1
    nsv3914470copy number variation1nstd102humanPathogenic GRCh37 chrX: 147,030,199-147,046,357 , GRCh38.p12 chrX: 147,948,679-147,964,837 FMR1
    nsv3909837copy number variation1nstd102humanPathogenic GRCh37.p13 chrX|NW_004070890.2: 3,432,726-3,436,286 , NCBI36 chrX: 146,797,545-146,801,105 , GRCh38 chrX: 147,908,335-147,911,895 FMR1, FMR1-AS1
    nsv997159copy number variation1nstd45humanPathogenic GRCh37 chrX: 146,993,469-147,032,647 , GRCh38.p12 chrX: 147,911,951-147,951,127 FMR1, FMR1-AS1
    nsv3883927copy number variation1nstd102humanPathogenic GRCh37 chr6: 146,735,206-147,036,914 , GRCh38 chr6: 146,414,070-146,715,778 ADGB, RAB32, 2 more genes
    nsv1398596copy number variation1nstd102humanPathogenic NCBI36 chrX: 146,703,942-146,820,448 , GRCh37.p13 chrX|NW_004070890.2: 3,339,123-3,455,629 , GRCh37.p13 chrX: 146,896,250-147,012,756 , GRCh38.p12 chrX: 147,814,732-147,931,237 FMR1, RNU6-382P, 2 more genes
    nsv6313825copy number variation1nstd102humanPathogenic GRCh37 chrX: 146,930,611-147,023,367 , GRCh38.p12 chrX: 147,849,093-147,941,848 FMR1, FMR1-AS1, 1 more genes
    nsv3887963copy number variation1nstd102humanUncertain significance GRCh37 chrX: 146,683,917-147,028,535 , GRCh38.p12 chrX: 147,602,399-147,947,015 FMR1, FMR1-AS1, 3 more genes
    nsv3885850copy number variation1nstd102humanUncertain significance GRCh37 chrX: 146,726,429-147,028,536 , GRCh38.p12 chrX: 147,644,911-147,947,016 FMR1, FMR1-AS1, 3 more genes
    nsv3887948copy number variation1nstd102humanUncertain significance GRCh37 chrX: 146,977,059-147,106,579 , GRCh38.p12 chrX: 147,895,541-148,025,059 FMR1, FMR1NB, 2 more genes
    nsv3917881copy number variation1nstd102humanPathogenic NCBI36 chrX: 146,558,195-147,126,824 , GRCh37.p13 chrX|NW_004070890.2: 3,193,376-3,762,005 , GRCh37.p13 chrX: 146,750,503-147,319,132 , GRCh38.p12 chrX: 147,668,985-148,237,612 FMR1, FTH1P8, 7 more genes
    nsv3904162copy number variation1nstd102humanPathogenic GRCh38 chrX: 10,001-156,030,895 , GRCh37 chrX: 60,001-155,260,560 , NCBI36 chrX: 1-154,913,754 FMR1, NANOGNBP3, 2154 more genes
    nsv3913255copy number variation2nstd102humanPathogenic NCBI36 chrX: 701-154,913,754 , GRCh37.p13 chrX: 60,701-155,260,560 , GRCh38.p12 chrX: 10,701-156,030,895 FMR1, NHS-AS1, 2154 more genes
    nsv3907094copy number variation4nstd102humanPathogenic GRCh38 chrX: 10,679-156,022,206 , GRCh37 chrX: 60,679-155,251,871 , NCBI36 chrX: 679-154,905,065 FMR1, GPR119, 2153 more genes
    nsv3878553copy number variation2nstd102humanPathogenic GRCh37 chrX: 60,262-155,245,765 , GRCh38.p12 chrX: 10,262-156,016,100 FMR1, H2AB2, 2152 more genes
    nsv3898149copy number variation1nstd102humanPathogenic GRCh38 chrX: 20,297-156,026,127 , NCBI36 chrX: 10,297-154,908,986 , GRCh37 chrX: 70,297-155,255,792 FMR1, OR3B1P, 2154 more genes
    nsv3877395copy number variation1nstd102humanPathogenic GRCh37 chrX: 71,267-155,255,839 , GRCh38.p12 chrX: 21,267-156,026,174 FMR1, ARMCX2, 2154 more genes
    nsv3884935copy number variation1nstd102humanPathogenic GRCh37 chrX: 71,267-155,255,792 , GRCh38.p12 chrX: 21,267-156,026,127 FMR1, NDUFB11, 2154 more genes
    nsv3903061copy number variation1nstd102humanPathogenic NCBI36 chrX: 679-154,896,026 , GRCh38 chrX: 10,679-156,013,167 , GRCh37 chrX: 60,679-155,242,832 FMR1, SLC38A5, 2152 more genes
    nsv3885865copy number variation1nstd102humanPathogenic GRCh37 chrX: 70,297-155,246,585 , GRCh38.p12 chrX: 20,297-156,016,920 FMR1, MIR1277, 2152 more genes
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