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Items: 1 to 20 of 120

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7057353inversion1nstd229human GRCh38 chr3: 51,679,548-51,681,937 , GRCh37.p13 chr3: 51,713,564-51,715,953 TEX264
    nsv7042459inversion1nstd229human GRCh38 chr3: 51,681,796-51,684,393 , GRCh37.p13 chr3: 51,715,812-51,718,409 TEX264
    nsv6711901copy number variation1nstd229human GRCh38 chr3: 51,682,005-51,682,202 , GRCh37.p13 chr3: 51,716,021-51,716,218 TEX264
    nsv6254006mobile element insertion1nstd215human GRCh38 chr3: 51,688,388-51,688,388 , GRCh37.p13 chr3: 51,722,404-51,722,404 TEX264
    nsv6135016copy number variation1nstd213human GRCh37 chr3: 48,760,000-52,290,001 , GRCh38.p12 chr3: 48,722,567-52,255,985 ACY1, ALAS1, 128 more genes
    nsv6134694copy number variation1nstd213human GRCh37 chr3: 46,170,000-52,140,001 , GRCh38.p12 chr3: 46,128,508-52,105,985 ACY1, AMT, 210 more genes
    nsv5994133copy number variation1nstd212human GRCh38 chr3: 51,694,006-51,694,096 , GRCh37.p13 chr3: 51,728,022-51,728,112 TEX264, RNA5SP132
    nsv5899644copy number variation1nstd209human GRCh38 chr3: 51,680,097-51,683,569 , GRCh37.p13 chr3: 51,714,113-51,717,585 TEX264
    nsv5891025copy number variation1nstd209human GRCh38 chr3: 49,693,626-52,462,904 , GRCh37.p13 chr3: 49,731,059-52,496,920 , SEMA3G, 106 more genes
    nsv5836369copy number variation1nstd209human GRCh38 chr3: 51,680,164-51,683,488 , GRCh37.p13 chr3: 51,714,180-51,717,504 TEX264
    nsv5561912sequence alteration1nstd206human GRCh38 chr3: 46,623,292-58,677,536 , GRCh37.p13 chr3: 46,664,782-58,663,263 , CDC25A, 327 more genes
    nsv5037434inversion1nstd200human GRCh38 chr3: 5,031,119-56,902,223 , GRCh37.p13 chr3: 5,072,804-56,936,251 , IRAK2, 925 more genes
    nsv5030280inversion1nstd200human GRCh38 chr3: 3,432,416-77,775,308 , GRCh37.p13 chr3: 3,474,100-77,824,459 , BHLHE40, 1198 more genes
    nsv4911344copy number variation1nstd200human GRCh38 chr3: 51,697,396-51,697,496 , GRCh37.p13 chr3: 51,731,412-51,731,512 TEX264
    nsv4888770inversion1nstd200human GRCh37 chr3: 3,474,100-77,824,459 , GRCh38.p12 chr3: 3,432,416-77,775,308 , ATRIP, 1198 more genes
    nsv4877503inversion1nstd200human GRCh37 chr3: 24,885,632-100,711,157 , GRCh38.p12 chr3: 24,844,141-100,992,313 , LINC00692, 1088 more genes
    nsv4790697copy number variation1nstd200human GRCh37 chr3: 51,731,412-51,731,512 , GRCh38.p12 chr3: 51,697,396-51,697,496 TEX264
    nsv4673975copy number variation1nstd102humanUncertain significance GRCh37 chr3: 51,247,306-53,069,942 , GRCh38.p12 chr3: 51,209,875-53,035,926 RRP9, LOC100301990, 76 more genes
    nsv4564128inversion1nstd166human GRCh37.p13 chr3: 3,474,047-77,824,459 , GRCh38.p12 chr3: 3,432,363-77,775,308 , ACY1, 1205 more genes
    nsv4347762copy number variation1nstd102humanPathogenic GRCh37 chr3: 45,153,770-53,878,616 , GRCh38.p12 chr3: 45,112,278-53,844,589 UQCRC1, DHX30, 291 more genes
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