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Items: 1 to 20 of 148

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5895968copy number variation1nstd209human GRCh38 chr3: 8,757,250-8,757,331 , GRCh37.p13 chr3: 8,798,936-8,799,017 OXTR
    nsv5438282copy number variation1nstd206human GRCh38 chr3: 8,757,252-8,757,332 , GRCh37.p13 chr3: 8,798,938-8,799,018 OXTR
    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
    nsv4888770inversion1nstd200human GRCh37 chr3: 3,474,100-77,824,459 , GRCh38.p12 chr3: 3,432,416-77,775,308 , ATRIP, 1198 more genes
    nsv4728170copy number variation1nstd102humanUncertain significance GRCh37 chr3: 8,745,819-9,043,663 , GRCh38.p12 chr3: 8,704,133-9,001,979 LOC107984112, LOC107986061, 5 more genes
    nsv4683387copy number variation1nstd102humanUncertain significance GRCh37 chr3: 8,775,553-9,730,776 , GRCh38.p12 chr3: 8,733,867-9,689,092 MTMR14, THUMPD3, 16 more genes
    nsv4674715copy number variation1nstd102humanPathogenic GRCh37 chr3: 61,891-10,287,825 , GRCh38.p12 chr3: 20,213-10,246,141 LOC105376944, LMCD1, 122 more genes
    nsv4674524copy number variation1nstd102humanUncertain significance GRCh37 chr3: 7,172,720-9,545,741 , GRCh38.p12 chr3: 7,131,033-9,504,057 SRGAP3-AS4, LOC101927394, 23 more genes
    nsv4674166copy number variation1nstd102humanUncertain significance GRCh37 chr3: 8,736,661-8,889,809 , GRCh38.p12 chr3: 8,694,975-8,848,125 OXTR, LOC107986061, 3 more genes
    nsv4637871copy number variation1nstd186human GRCh37 chr3: 8,798,938-8,799,018 , GRCh38.p12 chr3: 8,757,252-8,757,332 OXTR
    nsv4564128inversion1nstd166human GRCh37.p13 chr3: 3,474,047-77,824,459 , GRCh38.p12 chr3: 3,432,363-77,775,308 , ACY1, 1205 more genes
    nsv4436544copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 36,016-9,307,855 , GRCh38.p12 chr3: 18,324-9,266,171 CAV3, GRM7, 83 more genes
    nsv4322351inversion1nstd166human GRCh37.p13 chr3: 5,153,487-11,332,347 , GRCh38.p12 chr3: 5,111,802-11,290,661 CAV3, HRH1, 96 more genes
    nsv4080384copy number variation1nstd166human GRCh37.p13 chr3: 8,798,938-8,799,018 , GRCh38.p12 chr3: 8,757,252-8,757,332 OXTR
    nsv4078139copy number variation1nstd166human GRCh37.p13 chr3: 8,788,501-8,806,275 , GRCh38.p12 chr3: 8,746,815-8,764,589 OXTR, CAV3
    nsv3924579copy number variation1nstd102humanLikely pathogenic NCBI36 chr3: 8,055,414-11,257,617 , GRCh37 chr3: 8,080,414-11,282,617 , GRCh38 chr3: 8,038,727-11,240,931 ATP2B2, CAV3, 74 more genes
    nsv3922069copy number variation1nstd102humanLikely pathogenic NCBI36 chr3: 7,992,421-12,653,416 , GRCh37 chr3: 8,017,421-12,678,416 , GRCh38 chr3: 7,975,734-12,636,917 ATP2B2, CAV3, 96 more genes
    nsv3919362copy number variation1nstd102humanUncertain significance NCBI36 chr3: 7,992,421-9,054,817 , GRCh37 chr3: 8,017,421-9,079,817 , GRCh38 chr3: 7,975,734-9,038,133 LMCD1, LMCD1-AS1, 13 more genes
    nsv3918747copy number variation1nstd102humanPathogenic GRCh38 chr3: 8,320,124-9,395,968 , GRCh37 chr3: 8,361,812-9,437,652 , NCBI36 chr3: 8,336,812-9,412,652 THUMPD3, LOC107986061, 19 more genes
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