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Items: 1 to 20 of 288

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137157inversion1nstd234human GRCh37 chrX: 31,626,542-82,320,140 , GRCh38.p12 chrX: 31,608,425-83,065,132 ABCB7, ACTG1P10, 775 more genes
    nsv7137063copy number variation1nstd102humanPathogenic GRCh37 chrX: 200,855-155,240,074 , GRCh38.p12 chrX: 284,188-156,010,409 RN7SL581P, HMGB1P32, 2151 more genes
    nsv7089550copy number variation1nstd229human GRCh38 chrX: 81,414,001-81,436,800 , GRCh37.p13 chrX: 80,669,500-80,692,299 LOC100422471, LOC105373284
    nsv7089549copy number variation1nstd229human GRCh38 chrX: 81,407,752-81,419,086 , GRCh37.p13 chrX: 80,663,251-80,674,585 LOC105373284, LOC100422471
    nsv7089507copy number variation1nstd229human GRCh38 chrX: 81,045,335-81,839,994 , GRCh37.p13 chrX: 80,300,834-81,095,493 LOC105373284, LOC105373285, 4 more genes
    nsv7089457copy number variation1nstd229human GRCh38 chrX: 80,508,685-81,495,723 , GRCh37.p13 chrX: 79,764,184-80,751,222 LOC105373284, WBP11P3, 11 more genes
    nsv7034748inversion1nstd229human GRCh38 chrX: 80,442,808-84,464,579 , GRCh37.p13 chrX: 79,698,307-83,719,587 EIF3MP1, HDX, 28 more genes
    nsv7027974inversion1nstd229human GRCh38 chrX: 81,413,015-81,431,074 , GRCh37.p13 chrX: 80,668,514-80,686,573 LOC100422471, LOC105373284
    nsv6636960copy number variation1nstd102humanUncertain significance GRCh37 chrX: 80,404,540-81,278,950 , GRCh38.p12 chrX: 81,149,041-82,023,501 HMGN5, SH3BGRL, 5 more genes
    nsv6634329copy number variation1nstd102humanPathogenic GRCh37 chrX: 76,794,355-119,282,836 , GRCh38.p12 chrX: 77,538,874-120,148,930 NXF4, RHOXF1P1, 489 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
    nsv6315332copy number variation1nstd102humanPathogenic GRCh37 chrX: 62,685,885-155,233,731 , GRCh38.p12 chrX: 63,466,005-156,004,066 MAGT1, TAFAZZIN, 1337 more genes
    nsv6315331copy number variation4nstd102humanPathogenic GRCh37 chrX: 1-155,270,560 , GRCh38.p12 chrX: 10,001-156,030,895 PLAC1, PGK1P1, 2154 more genes
    nsv6314938copy number variation1nstd102humanUncertain significance GRCh37 chrX: 79,979,500-81,247,449 , GRCh38.p12 chrX: 80,724,001-81,992,000 HMGN5, SH3BGRL, 8 more genes
    nsv6313469copy number variation1nstd102humanPathogenic GRCh37 chrX: 78,104,966-86,189,374 , GRCh38.p12 chrX: 78,849,469-86,934,371 MIR361, TERF1P4, 59 more genes
    nsv6313464copy number variation1nstd102humanUncertain significance GRCh37 chrX: 72,095,006-88,455,505 , GRCh38.p12 chrX: 72,875,172-89,200,506 LOC105373285, LOC105373288, 170 more genes
    nsv6290670copy number variation1nstd102humanUncertain significance GRCh37 chrX: 78,558,916-86,314,970 , GRCh38.p12 chrX: 79,303,419-87,059,967 LOC105373284, RNU6-995P, 54 more genes
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