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Items: 1 to 20 of 309

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137063copy number variation1nstd102humanPathogenic GRCh37 chrX: 200,855-155,240,074 , GRCh38.p12 chrX: 284,188-156,010,409 RN7SL581P, HMGB1P32, 2151 more genes
    nsv7090952copy number variation1nstd229human GRCh38 chrX: 126,162,401-126,166,200 , GRCh37.p13 chrX: 125,296,384-125,300,183 DCAF12L2
    nsv7090951copy number variation1nstd229human GRCh38 chrX: 126,156,846-126,377,526 , GRCh37.p13 chrX: 125,290,829-125,511,509 DCAF12L2, LOC107985648
    nsv7090946copy number variation1nstd229human GRCh38 chrX: 126,150,103-126,256,242 , GRCh37.p13 chrX: 125,284,086-125,390,225 DCAF12L2, LOC107985648
    nsv7090930copy number variation1nstd229human GRCh38 chrX: 126,141,192-126,537,678 , GRCh37.p13 chrX: 125,275,175-125,671,661 DCAF12L2, OR4W1P, 4 more genes
    nsv7090928copy number variation1nstd229human GRCh38 chrX: 126,137,318-126,472,157 , GRCh37.p13 chrX: 125,271,301-125,606,140 MTCO1P53, LOC107985648, 3 more genes
    nsv7090923copy number variation1nstd229human GRCh38 chrX: 126,099,101-126,190,109 , GRCh37.p13 chrX: 125,233,084-125,324,092 LOC101928495, DCAF12L2
    nsv7090904copy number variation1nstd229human GRCh38 chrX: 125,987,612-126,175,628 , GRCh37.p13 chrX: 125,121,594-125,309,611 LOC101928495, DCAF12L2
    nsv7090900copy number variation1nstd229human GRCh38 chrX: 125,980,514-126,200,757 , GRCh37.p13 chrX: 125,114,496-125,334,740 LOC107985648, DCAF12L2, 1 more genes
    nsv7090864copy number variation1nstd229human GRCh38 chrX: 125,772,800-126,496,799 , GRCh37.p13 chrX: 124,906,782-125,630,782 LOC101928495, LOC107985648, 4 more genes
    nsv7090861copy number variation1nstd229human GRCh38 chrX: 125,767,892-126,314,395 , GRCh37.p13 chrX: 124,901,874-125,448,378 DCAF12L2, LOC101928495, 1 more genes
    nsv7090822copy number variation1nstd229human GRCh38 chrX: 125,372,816-126,495,112 , GRCh37.p13 chrX: 124,506,665-125,629,095 LOC107985648, MTND4P24, 4 more genes
    nsv7083371copy number variation1nstd229human GRCh38 chrX: 121,591,286-126,454,661 , GRCh37.p13 chrX: 120,725,140-125,588,644 RNU7-69P, SH2D1A, 31 more genes
    nsv7051160inversion1nstd229human GRCh38 chrX: 125,928,400-126,327,917 , GRCh37.p13 chrX: 125,062,382-125,461,900 LOC107985648, DCAF12L2, 1 more genes
    nsv7044497inversion1nstd229human GRCh38 chrX: 125,641,422-126,317,788 , GRCh37.p13 chrX: 124,775,421-125,451,771 LOC107985648, DCAF12L2, 1 more genes
    nsv6636407copy number variation1nstd102humanPathogenic GRCh37 chrX: 124,749,464-155,233,731 , GRCh38.p12 chrX: 125,615,468-156,004,066 RN7SKP31, LOC728470, 539 more genes
    nsv6634242copy number variation1nstd224human GRCh37 chrX: 1-155,270,560 , GRCh38.p12 chrX: 10,001-156,030,895 NR0B1, ALAS2, 2154 more genes
    nsv6315429copy number variation1nstd102humanPathogenic GRCh37 chrX: 77,670,699-155,233,731 , GRCh38.p12 chrX: 78,415,202-156,004,066 H2AB1, GPR174, 1081 more genes
    nsv6315393copy number variation1nstd102humanPathogenic GRCh37 chrX: 61,545-155,226,048 , GRCh38.p12 chrX: 11,545-155,996,383 H2BP8, LOC101060199, 2151 more genes
    nsv6315389copy number variation1nstd102humanPathogenic GRCh37 chrX: 11,522,765-155,233,731 , GRCh38.p12 chrX: 11,504,645-156,004,066 RBMX, LOC100129144, 2042 more genes
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