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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
    nsv7098588copy number variation1nstd102humanUncertain significance GRCh37 chrX: 135,080,247-135,126,903 , GRCh38.p12 chrX: 135,998,088-136,044,744 SLC9A6
    nsv7098345copy number variation1nstd102humanPathogenic GRCh37 chrX: 135,104,725-135,104,876 , GRCh38.p12 chrX: 136,022,566-136,022,717 SLC9A6
    nsv7098229copy number variation1nstd102humanPathogenic GRCh37 chrX: 135,104,725-135,106,662 , GRCh38.p12 chrX: 136,022,566-136,024,503 SLC9A6
    nsv7084239copy number variation1nstd229human GRCh38 chrX: 136,045,755-136,045,961 , GRCh37.p13 chrX: 135,127,914-135,128,120 , GRCh37.p13 chrX|NW_004070887.1: 976,898-977,104 SLC9A6
    nsv7084238copy number variation1nstd229human GRCh38 chrX: 136,039,934-136,040,127 , GRCh37.p13 chrX: 135,122,093-135,122,286 , GRCh37.p13 chrX|NW_004070887.1: 971,077-971,270 SLC9A6
    nsv7084237copy number variation1nstd229human GRCh38 chrX: 136,036,234-136,038,996 , GRCh37.p13 chrX: 135,118,393-135,121,155 , GRCh37.p13 chrX|NW_004070887.1: 967,377-970,139 SLC9A6
    nsv7084236copy number variation1nstd229human GRCh38 chrX: 136,033,128-136,033,367 , GRCh37.p13 chrX: 135,115,287-135,115,526 , GRCh37.p13 chrX|NW_004070887.1: 964,271-964,510 SLC9A6
    nsv7084235copy number variation1nstd229human GRCh38 chrX: 136,030,640-136,031,167 , GRCh37.p13 chrX|NW_004070887.1: 961,783-962,310 , GRCh37.p13 chrX: 135,112,799-135,113,326 SLC9A6
    nsv7084234copy number variation1nstd229human GRCh38 chrX: 136,020,321-136,020,374 , GRCh37.p13 chrX|NW_004070887.1: 951,464-951,517 , GRCh37.p13 chrX: 135,102,480-135,102,533 SLC9A6
    nsv7084233copy number variation1nstd229human GRCh38 chrX: 135,977,329-135,977,534 , GRCh37.p13 chrX|NW_004070887.1: 908,472-908,677 , GRCh37.p13 chrX: 135,059,488-135,059,693 SLC9A6
    nsv7084229copy number variation1nstd229human GRCh38 chrX: 135,934,637-135,982,599 , GRCh37.p13 chrX: 135,016,796-135,064,758 , GRCh37.p13 chrX|NW_004070887.1: 865,780-913,742 MMGT1, CT45A11P, 1 more genes
    nsv7045979inversion1nstd229human GRCh38 chrX: 135,998,507-135,998,541 , GRCh37.p13 chrX|NW_004070887.1: 929,650-929,684 , GRCh37.p13 chrX: 135,080,666-135,080,700 SLC9A6
    nsv7044060inversion1nstd229human GRCh38 chrX: 134,736,748-136,484,102 , GRCh37.p13 chrX|NW_004070887.1: 1-1,045,622 , GRCh37.p13 chrX: 133,870,778-135,566,261 ETDA, SAGE3P, 57 more genes
    nsv6636956copy number variation1nstd102humanUncertain significance GRCh37 chrX: 135,017,562-135,489,217 , GRCh38.p12 chrX: 135,935,403-136,407,058 SLC9A6, ADGRG4, 7 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
    nsv6633775copy number variation1nstd224human GRCh37 chrX: 133,906,202-135,831,362 , GRCh38.p12 chrX: 134,772,172-136,749,203 GAPDHP67, VGLL1, 63 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
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