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Items: 1 to 20 of 164

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5890710copy number variation1nstd209human GRCh38 chr3: 58,306,665-58,306,754 , GRCh37.p13 chr3: 58,292,392-58,292,481 RPP14, HTD2
    nsv5727202mobile element insertion1nstd211human GRCh38 chr3: 58,322,759-58,322,759 , GRCh37.p13 chr3: 58,308,486-58,308,486 RPP14
    nsv5561912sequence alteration1nstd206human GRCh38 chr3: 46,623,292-58,677,536 , GRCh37.p13 chr3: 46,664,782-58,663,263 , CDC25A, 327 more genes
    nsv5558076mobile element insertion1nstd206human GRCh38 chr3: 58,322,759-58,322,810 , GRCh37.p13 chr3: 58,308,486-58,308,537 RPP14
    nsv5446715copy number variation1nstd206human GRCh38 chr3: 58,306,665-58,306,755 , GRCh37.p13 chr3: 58,292,392-58,292,482 RPP14, HTD2
    nsv5309719copy number variation1nstd204human GRCh37.p13 chr3: 58,258,018-58,300,101 , GRCh38.p13 chr3: 58,272,291-58,314,374 RPP14, ABHD6, 1 more genes
    nsv5217810copy number variation1nstd204human GRCh38.p13 chr3: 58,271,802-58,307,198 , GRCh37.p13 chr3: 58,257,529-58,292,925 ABHD6, HTD2, 1 more genes
    nsv5202994copy number variation1nstd204human GRCh38.p13 chr3: 58,303,766-58,304,865 , GRCh37.p13 chr3: 58,289,493-58,290,592 RPP14, HTD2
    nsv5030280inversion1nstd200human GRCh38 chr3: 3,432,416-77,775,308 , GRCh37.p13 chr3: 3,474,100-77,824,459 , BHLHE40, 1198 more genes
    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
    nsv4728391copy number variation1nstd102humanUncertain significance GRCh37 chr3: 57,912,545-58,357,970 , GRCh38.p12 chr3: 57,926,818-58,372,243 SLMAP, ABHD6, 10 more genes
    nsv4680923copy number variation1nstd189human GRCh37.p13 chr3: 58,307,061-58,409,731 , GRCh38.p12 chr3: 58,321,334-58,424,004 RPP14, PXK, 1 more genes
    nsv4680755copy number variation1nstd189human GRCh37.p13 chr3: 58,090,932-58,319,338 , GRCh38.p12 chr3: 58,105,205-58,333,611 , DNASE1L3, 7 more genes
    nsv4679214copy number variation1nstd189human GRCh37.p13 chr3: 58,281,492-58,408,851 , GRCh38.p12 chr3: 58,295,765-58,423,124 RPP14, PXK, 2 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
    nsv4542926insertion1nstd166human GRCh37.p13 chr3: 58,292,391-58,292,391 , GRCh38.p12 chr3: 58,306,664-58,306,664 RPP14, HTD2
    nsv4452524copy number variation1nstd102humanPathogenic GRCh37 chr3: 57,076,136-65,716,956 , GRCh38.p12 chr3: 57,042,108-65,731,281 LOC105377114, FAM107A, 110 more genes
    nsv4087160copy number variation1nstd166human GRCh37.p13 chr3: 58,292,392-58,292,482 , GRCh38.p12 chr3: 58,306,665-58,306,755 HTD2, RPP14
    nsv3921125copy number variation1nstd102humanUncertain significance GRCh37 chr3: 57,897,017-58,395,655 , NCBI36 chr3: 57,872,057-58,370,695 , GRCh38 chr3: 57,911,290-58,409,928 HTD2, FLNB-AS1, 11 more genes
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