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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6311980copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr3: 3,170,725-3,189,838 , GRCh38.p12 chr3: 3,129,041-3,148,154 CRBN, TRNT1
    nsv7096460copy number variation1nstd102humanPathogenic GRCh37 chr3: 3,186,248-3,189,838 , GRCh38.p12 chr3: 3,144,564-3,148,154 CRBN, TRNT1
    nsv6311981copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 3,179,743-3,189,406 , GRCh38.p12 chr3: 3,138,059-3,147,722 CRBN, TRNT1
    nsv4682673copy number variation1nstd102humanUncertain significance GRCh37 chr3: 3,170,705-3,189,858 , GRCh38.p12 chr3: 3,129,021-3,148,174 CRBN, TRNT1
    nsv3904614copy number variation1nstd102humanUncertain significance GRCh37 chr3: 3,101,824-3,304,982 , NCBI36 chr3: 3,076,824-3,279,982 , GRCh38 chr3: 3,060,140-3,263,298 CRBN, IL5RA, 2 more genes
    nsv4674244copy number variation1nstd102humanUncertain significance GRCh37 chr3: 3,136,087-3,692,515 , GRCh38.p12 chr3: 3,094,403-3,650,831 CRBN, IL5RA, 1 more genes
    nsv3905232copy number variation1nstd102humanPathogenic GRCh38 chr3: 32,241-12,681,483 , GRCh37 chr3: 73,914-12,722,982 , NCBI36 chr3: 48,914-12,697,982 CRBN, OR7E122P, 163 more genes
    nsv3885461copy number variation1nstd102humanPathogenic GRCh37 chr3: 61,891-12,575,409 , GRCh38.p12 chr3: 20,213-12,533,910 CRBN, MARK2P14, 160 more genes
    nsv6636276copy number variation1nstd102humanPathogenic GRCh37 chr3: 61,892-11,679,509 , GRCh38.p12 chr3: 20,214-11,638,035 CRBN, RPL23AP39, 144 more genes
    nsv3906827copy number variation1nstd102humanPathogenic GRCh38 chr3: 32,241-11,379,835 , GRCh37 chr3: 73,914-11,421,309 , NCBI36 chr3: 48,914-11,396,309 CRBN, LOC107986040, 142 more genes
    nsv3895550copy number variation1nstd102humanPathogenic GRCh38 chr3: 20,213-11,221,602 , NCBI36 chr3: 36,891-11,238,288 , GRCh37 chr3: 61,891-11,263,288 CRBN, SRGAP3, 141 more genes
    nsv3900952copy number variation1nstd102humanPathogenic GRCh38 chr3: 52,266-11,089,569 , NCBI36 chr3: 68,949-11,106,255 , GRCh37 chr3: 93,949-11,131,255 CRBN, RPUSD3, 137 more genes
    nsv3900980copy number variation1nstd102humanPathogenic GRCh37 chr3: 73,914-10,672,995 , GRCh38 chr3: 32,241-10,631,310 , NCBI36 chr3: 48,914-10,647,995 CRBN, MIR885, 131 more genes
    nsv3892568copy number variation1nstd102humanPathogenic NCBI36 chr3: 705,581-11,067,828 , GRCh37 chr3: 730,581-11,092,828 , GRCh38 chr3: 688,897-11,051,142 CRBN, DUSP5P2, 126 more genes
    nsv3894686copy number variation1nstd102humanPathogenic NCBI36 chr3: 48,914-10,339,808 , GRCh38 chr3: 32,241-10,323,124 , GRCh37 chr3: 73,914-10,364,808 CRBN, RPL21P17, 128 more genes
    nsv4674715copy number variation1nstd102humanPathogenic GRCh37 chr3: 61,891-10,287,825 , GRCh38.p12 chr3: 20,213-10,246,141 CRBN, LOC105376944, 122 more genes
    nsv3889023copy number variation1nstd102humanPathogenic GRCh37 chr3: 61,891-10,104,842 , GRCh38.p12 chr3: 20,213-10,063,158 CRBN, TTLL3, 118 more genes
    nsv6636296copy number variation1nstd102humanPathogenic GRCh37 chr3: 61,892-9,899,605 , GRCh38.p12 chr3: 20,214-9,857,921 CRBN, GRM7-AS1, 101 more genes
    nsv6313525copy number variation1nstd102humanPathogenic GRCh37 chr3: 61,891-9,797,094 , GRCh38.p12 chr3: 20,213-9,755,410 CRBN, EGOT, 95 more genes
    nsv6636323copy number variation1nstd102humanPathogenic GRCh37 chr3: 61,892-9,769,457 , GRCh38.p12 chr3: 20,214-9,727,773 CRBN, LOC107984112, 92 more genes
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