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Items: 1 to 20 of 167

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5892310copy number variation1nstd209human GRCh38 chr3: 58,498,556-58,498,662 , GRCh37.p13 chr3: 58,484,283-58,484,389 KCTD6
    nsv5561912sequence alteration1nstd206human GRCh38 chr3: 46,623,292-58,677,536 , GRCh37.p13 chr3: 46,664,782-58,663,263 , CDC25A, 327 more genes
    nsv5030280inversion1nstd200human GRCh38 chr3: 3,432,416-77,775,308 , GRCh37.p13 chr3: 3,474,100-77,824,459 , BHLHE40, 1198 more genes
    nsv4924456copy number variation1nstd200human GRCh38 chr3: 58,502,340-60,224,074 , GRCh37.p13 chr3: 58,488,067-60,209,802 LOC105377109, SNRPB2P1, 14 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
    nsv4588798copy number variation1nstd183human GRCh37 chr3: 58,477,601-58,478,135 , GRCh38.p12 chr3: 58,491,874-58,492,408 KCTD6
    nsv4586470copy number variation1nstd183human GRCh37 chr3: 58,477,127-58,478,421 , GRCh38.p12 chr3: 58,491,400-58,492,694 KCTD6
    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
    nsv4400790copy number variation1nstd174human GRCh37 chr3: 58,477,127-58,478,421 , GRCh38.p12 chr3: 58,491,400-58,492,694 KCTD6
    nsv4377588copy number variation1nstd173human GRCh37 chr3: 58,484,521-60,210,851 , GRCh38.p12 chr3: 58,498,794-60,225,123 FHIT, ACOX2, 14 more genes
    nsv3958440copy number variation1nstd168human GRCh38 chr3: 58,496,595-58,573,602 , GRCh37.p13 chr3: 58,482,322-58,559,329 LOC107984079, KCTD6, 3 more genes
    nsv3922342copy number variation1nstd102humanUncertain significance NCBI36 chr3: 58,459,560-60,177,941 , GRCh37 chr3: 58,484,520-60,202,901 , GRCh38 chr3: 58,498,793-60,217,173 LOC105377112, SNRPB2P1, 14 more genes
    nsv3919181copy number variation1nstd102humanPathogenic GRCh38 chr3: 54,045,018-66,060,461 , GRCh37 chr3: 54,079,045-66,046,136 , NCBI36 chr3: 54,054,085-66,021,176 MAGI1-AS1, FEZF2, 135 more genes
    nsv3917204copy number variation1nstd102humanPathogenic GRCh38 chr3: 57,430,538-64,884,522 , NCBI36 chr3: 57,391,305-64,845,237 , GRCh37 chr3: 57,416,265-64,870,197 C3orf49, PPIAP16, 93 more genes
    nsv3916461copy number variation1nstd102humanPathogenic GRCh37 chr3: 57,174,452-90,309,110 , NCBI36 chr3: 57,149,492-90,391,800 , GRCh38 chr3: 57,140,424-90,259,960 LOC105377171, HNRNPA3P6, 323 more genes
    nsv3889228copy number variation2nstd102humanPathogenic GRCh37 chr3: 61,892-197,851,986 , GRCh38.p12 chr3: 20,214-198,125,115 NDUFB4, LOC105374108, 2876 more genes
    nsv3886371copy number variation1nstd102humanBenign GRCh37 chr3: 58,089,516-58,799,748 , GRCh38.p12 chr3: 58,103,789-58,814,022 ACOX2, ABHD6, 18 more genes
    nsv3885606copy number variation1nstd102humanPathogenic GRCh37 chr3: 60,174-197,948,027 , GRCh38.p12 chr3: 18,496-198,221,156 RNU4-62P, SEMA3B-AS1, 2880 more genes
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