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Items: 1 to 20 of 123

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7051968inversion1nstd229human GRCh38 chr3: 56,944,702-65,952,705 , GRCh37.p13 chr3: 56,978,730-65,938,380 ILF2P1, ARHGEF3-AS1, 115 more genes
    nsv7048271inversion1nstd229human GRCh38 chr3: 59,959,176-65,947,271 , GRCh37.p13 chr3: 59,944,902-65,932,946 LOC105377124, RPS10P10, 63 more genes
    nsv7039673inversion1nstd229human GRCh38 chr3: 59,959,184-65,957,254 , GRCh37.p13 chr3: 59,944,910-65,942,929 PPIAP70, LOC105377114, 63 more genes
    nsv6713042copy number variation1nstd229human GRCh38 chr3: 64,185,328-64,185,547 , GRCh37.p13 chr3: 64,171,004-64,171,223 PRICKLE2-AS3, PRICKLE2
    nsv6705972copy number variation1nstd229human GRCh38 chr3: 64,200,594-64,202,815 , GRCh37.p13 chr3: 64,186,270-64,188,491 PRICKLE2, PRICKLE2-AS3
    nsv6703058copy number variation1nstd229human GRCh38 chr3: 64,159,924-64,543,048 , GRCh37.p13 chr3: 64,145,600-64,528,724 PRICKLE2-AS3, ADAMTS9, 5 more genes
    nsv6358374copy number variation1nstd223human GRCh38 chr3: 64,200,012-64,200,691 , GRCh37.p13 chr3: 64,185,688-64,186,367 PRICKLE2-AS3, PRICKLE2
    nsv6290933copy number variation1nstd102humanPathogenic GRCh37 chr3: 59,332,508-70,686,155 , GRCh38.p12 chr3: 59,346,782-70,637,004 NDUFB4P1, UBA3, 110 more genes
    nsv6134701copy number variation1nstd213human GRCh37 chr3: 63,610,000-66,170,001 , GRCh38.p12 chr3: 63,624,324-66,184,326 ATXN7, MAGI1, 36 more genes
    nsv6134696copy number variation1nstd213human GRCh37 chr3: 60,070,000-66,170,001 , GRCh38.p12 chr3: 60,084,274-66,184,326 FHIT, PTPRG, 65 more genes
    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
    nsv4674306copy number variation1nstd102humanPathogenic GRCh37 chr3: 60,449,667-65,561,638 , GRCh38.p12 chr3: 60,463,934-65,575,963 THOC7-AS1, LOC105377647, 56 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
    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
    nsv4088492copy number variation1nstd166human GRCh37.p13 chr3: 64,183,284-64,183,380 , GRCh38.p12 chr3: 64,197,608-64,197,704 PRICKLE2, PRICKLE2-AS3
    nsv4080334copy number variation1nstd166human GRCh37.p13 chr3: 64,181,756-64,182,547 , GRCh38.p12 chr3: 64,196,080-64,196,871 PRICKLE2-AS3, PRICKLE2
    nsv3922383copy number variation1nstd102humanPathogenic GRCh37 chr3: 61,956,521-68,514,983 , NCBI36 chr3: 61,931,561-68,597,673 , GRCh38 chr3: 61,970,847-68,465,832 UBL5P3, PRICKLE2-DT, 73 more genes
    nsv3920449copy number variation1nstd102humanUncertain significance GRCh38 chr3: 63,822,831-64,433,817 , NCBI36 chr3: 63,783,547-64,394,533 , GRCh37 chr3: 63,808,507-64,419,493 ATXN7, THOC7, 12 more genes
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