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Items: 1 to 20 of 449

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148184copy number variation1nstd102humanPathogenic GRCh38 chr1: 243,221,458-248,919,110 , GRCh37.p13 chr1: 243,384,760-249,213,309 LOC105373271, LOC107985725, 153 more genes
    nsv7098854copy number variation1nstd102humanPathogenic GRCh37 chr1: 245,704,069-249,212,562 , GRCh38.p12 chr1: 245,540,767-248,918,363 OR2X1P, OR14A2, 118 more genes
    nsv7055624inversion1nstd229human GRCh38 chr1: 248,905,750-248,917,534 , GRCh37.p13 chr1: 249,199,949-249,211,733 RNU6-1205P, PGBD2
    nsv7050661inversion1nstd229human GRCh38 chr1: 248,905,453-248,915,867 , GRCh37.p13 chr1: 249,199,652-249,210,066 PGBD2, RNU6-1205P
    nsv7047322inversion1nstd229human GRCh38 chr1: 248,745,368-248,877,498 , GRCh37.p13 chr1: 249,098,884-249,171,697 TRE-CTC2-1, ZNF692, 7 more genes
    nsv7044650inversion1nstd229human GRCh38 chr1: 248,874,037-248,895,527 , GRCh37.p13 chr1: 249,168,236-249,189,726 TRE-CTC2-1, PGBD2, 1 more genes
    nsv7041652inversion1nstd229human GRCh38 chr1: 248,859,961-248,871,868 , GRCh37.p13 chr1: 249,154,160-249,166,067 PGBD2, ZNF692, 1 more genes
    nsv6675941copy number variation1nstd229human GRCh38 chr1: 248,868,201-248,956,422 , GRCh37.p13 chr1: 249,162,400-249,240,621 PGBD2, TRE-CTC2-1, 3 more genes
    nsv6675512copy number variation1nstd229human GRCh38 chr1: 248,892,318-248,907,976 , GRCh37.p13 chr1: 249,186,517-249,202,175 PGBD2
    nsv6675304copy number variation1nstd229human GRCh38 chr1: 248,882,313-248,888,304 , GRCh37.p13 chr1: 249,176,512-249,182,503 PGBD2
    nsv6674268copy number variation1nstd229human GRCh38 chr1: 248,874,534-248,877,463 , GRCh37.p13 chr1: 249,168,733-249,171,662 TRE-CTC2-1, PGBD2
    nsv6673586copy number variation1nstd229human GRCh38 chr1: 248,867,901-248,956,422 , GRCh37.p13 chr1: 249,162,100-249,240,621 PGBD2, TRE-CTC2-1, 3 more genes
    nsv6673331copy number variation1nstd229human GRCh38 chr1: 248,794,344-248,887,696 , GRCh37.p13 chr1: 249,098,884-249,181,895 ZNF692, TRL-CAA4-1, 5 more genes
    nsv6672929copy number variation1nstd229human GRCh38 chr1: 248,877,679-248,883,034 , GRCh37.p13 chr1: 249,171,878-249,177,233 PGBD2
    nsv6672537copy number variation1nstd229human GRCh38 chr1: 248,917,501-248,923,600 , GRCh37.p13 chr1: 249,211,700-249,217,799 PGBD2
    nsv6671199copy number variation1nstd229human GRCh38 chr1: 248,866,484-248,872,903 , GRCh37.p13 chr1: 249,160,683-249,167,102 TRL-CAA4-1, PGBD2, 1 more genes
    nsv6670449copy number variation1nstd229human GRCh38 chr1: 248,873,068-248,873,120 , GRCh37.p13 chr1: 249,167,267-249,167,319 TRL-CAA4-1, PGBD2, 1 more genes
    nsv6670153copy number variation1nstd229human GRCh38 chr1: 248,874,244-248,878,165 , GRCh37.p13 chr1: 249,168,443-249,172,364 TRE-CTC2-1, PGBD2, 1 more genes
    nsv6668845copy number variation1nstd229human GRCh38 chr1: 248,875,811-248,883,031 , GRCh37.p13 chr1: 249,170,010-249,177,230 PGBD2
    nsv6667549copy number variation1nstd229human GRCh38 chr1: 248,867,801-248,956,422 , GRCh37.p13 chr1: 249,162,000-249,240,621 RPL23AP25, RNU6-1205P, 3 more genes
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