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Items: 1 to 20 of 283

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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
    nsv7083589copy number variation1nstd229human GRCh38 chrX: 123,563,801-123,569,800 , GRCh37.p13 chrX: 122,697,652-122,703,651 TUBB4AP1
    nsv7083585copy number variation1nstd229human GRCh38 chrX: 123,467,601-123,596,500 , GRCh37.p13 chrX: 122,601,452-122,730,351 H3P47, GRIA3, 2 more genes
    nsv7083581copy number variation1nstd229human GRCh38 chrX: 123,421,675-123,587,909 , GRCh37.p13 chrX: 122,555,526-122,721,760 GRIA3, TUBB4AP1, 2 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
    nsv6634242copy number variation1nstd224human GRCh37 chrX: 1-155,270,560 , GRCh38.p12 chrX: 10,001-156,030,895 NR0B1, ALAS2, 2154 more genes
    nsv6634194copy number variation1nstd224human GRCh37 chrX: 122,602,599-122,729,614 , GRCh38.p12 chrX: 123,468,748-123,595,763 GRIA3, TUBB4AP1, 2 more genes
    nsv6633759copy number variation1nstd224human GRCh37 chrX: 122,536,930-122,999,047 , GRCh38.p12 chrX: 123,403,079-123,865,197 XIAP, GRIA3, 9 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
    nsv6315159copy number variation1nstd102humanPathogenic GRCh38 chrX: 123,221,813-124,917,630 , GRCh37.p13 chrX: 122,355,664-124,051,479 STAG2-AS1, FERP1, 21 more genes
    nsv6313138copy number variation3nstd102humanUncertain significance, Pathogenic GRCh37 chrX: 122,318,388-123,505,241 , GRCh38.p12 chrX: 123,184,536-124,371,391 TEX13D, RN7SL190P, 18 more genes
    nsv6290546copy number variation1nstd102humanPathogenic GRCh37 chrX: 119,173,583-126,584,360 , GRCh38.p12 chrX: 120,039,618-127,450,379 FBLIM1P1, PNPLA10P, 81 more genes
    nsv6138208copy number variation1nstd206human GRCh38 chrX: 123,503,381-123,673,381 , GRCh37.p13 chrX: 122,637,232-122,807,232 THOC2, TUBB4AP1, 3 more genes
    nsv6137629copy number variation1nstd213human GRCh37 chrX: 66,030,000-152,230,001 , GRCh38.p12 chrX: 66,810,158-153,061,271 ABCB7, AGTR2, 1162 more genes
    nsv6137579copy number variation1nstd213human GRCh37 chrX: 114,940,000-134,860,001 , GRCh38.p12 chrX: 115,705,680-135,719,285 AGTR2, SLC25A5, 295 more genes
    nsv6137409copy number variation1nstd213human GRCh37 chrX: 73,710,000-151,990,001 , GRCh38.p12 chrX: 74,490,165-152,821,457 ABCB7, AGTR2, 991 more genes
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