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Items: 1 to 20 of 49

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6311973copy number variation1nstd102humanUncertain significance GRCh37 chr3: 191,074,857-191,109,549 , GRCh38.p12 chr3: 191,357,068-191,391,760 CCDC50
    nsv3884122copy number variation1nstd102humanBenign GRCh37 chr3: 191,045,551-191,070,810 , GRCh38.p12 chr3: 191,327,762-191,353,021 CCDC50, UTS2B
    nsv3912740copy number variation1nstd102humanUncertain significance GRCh37 chr3: 191,040,173-191,102,285 , GRCh38 chr3: 191,322,384-191,384,496 , NCBI36 chr3: 192,522,867-192,584,979 CCDC50, UTS2B
    nsv3910370copy number variation1nstd102humanUncertain significance NCBI36 chr3: 192,436,061-192,900,757 , GRCh38 chr3: 191,235,578-191,700,274 , GRCh37 chr3: 190,953,367-191,418,063 CCDC50, UTS2B, 3 more genes
    nsv3911287copy number variation1nstd102humanUncertain significance GRCh37 chr3: 191,037,181-191,261,730 , NCBI36 chr3: 192,519,875-192,744,424 , GRCh38 chr3: 191,319,392-191,543,941 CCDC50, PYDC2, 2 more genes
    nsv4728398copy number variation1nstd102humanUncertain significance GRCh37 chr3: 190,968,757-191,112,636 , GRCh38.p12 chr3: 191,250,968-191,394,847 CCDC50, OSTN, 1 more genes
    nsv3915488copy number variation1nstd102humanPathogenic GRCh37 chr3: 185,203,637-197,837,049 , NCBI36 chr3: 186,686,331-199,321,446 , GRCh38 chr3: 185,485,849-198,110,178 CCDC50, SNAR-I, 260 more genes
    nsv3914166copy number variation1nstd102humanPathogenic GRCh37 chr3: 180,856,452-192,229,812 , GRCh38 chr3: 181,138,664-192,512,023 , NCBI36 chr3: 182,339,146-193,712,506 CCDC50, SNORA4, 199 more genes
    nsv3920607copy number variation1nstd102humanPathogenic NCBI36 chr3: 187,082,628-197,946,692 , GRCh37.p13 chr3: 185,599,934-196,462,295 , GRCh38.p12 chr3: 185,882,146-196,735,424 CCDC50, FGF12, 212 more genes
    nsv3872972copy number variation1nstd102humanPathogenic GRCh37 chr3: 189,101,446-197,838,262 , GRCh38.p12 chr3: 189,383,657-198,111,391 CCDC50, TMEM44, 187 more genes
    nsv3882335copy number variation1nstd102humanPathogenic GRCh37 chr3: 182,650,681-191,275,809 , GRCh38.p12 chr3: 182,932,893-191,558,020 CCDC50, VPS8, 171 more genes
    nsv6290259copy number variation1nstd102humanPathogenic GRCh37 chr3: 189,608,636-197,532,175 , GRCh38.p12 chr3: 189,890,847-197,805,304 CCDC50, LINC01972, 174 more genes
    nsv3918718copy number variation1nstd102humanPathogenic GRCh37 chr3: 186,482,937-194,130,145 , NCBI36 chr3: 187,965,631-195,611,434 , GRCh38 chr3: 186,765,148-194,409,416 CCDC50, TPRG1-AS1, 114 more genes
    nsv3920718copy number variation1nstd102humanPathogenic NCBI36 chr3: 188,646,713-196,231,151 , GRCh37 chr3: 187,164,019-194,749,862 , GRCh38 chr3: 187,446,231-195,029,133 CCDC50, LOC105374283, 105 more genes
    nsv3885606copy number variation1nstd102humanPathogenic GRCh37 chr3: 60,174-197,948,027 , GRCh38.p12 chr3: 18,496-198,221,156 CCDC50, RNU4-62P, 2880 more genes
    nsv3889228copy number variation2nstd102humanPathogenic GRCh37 chr3: 61,892-197,851,986 , GRCh38.p12 chr3: 20,214-198,125,115 CCDC50, NDUFB4, 2876 more genes
    nsv3880617copy number variation1nstd102humanPathogenic GRCh37 chr3: 61,495-197,838,262 , GRCh38.p12 chr3: 19,817-198,111,391 CCDC50, RPL23AP49, 2875 more genes
    nsv3918981copy number variation1nstd102humanPathogenic GRCh37 chr3: 103,145,726-197,837,049 , GRCh38 chr3: 103,426,882-198,110,178 , NCBI36 chr3: 104,628,416-199,321,446 CCDC50, LINC02614, 1469 more genes
    nsv3918692copy number variation1nstd102humanPathogenic GRCh38 chr3: 147,521,892-198,096,565 , GRCh37 chr3: 147,239,679-197,823,436 , NCBI36 chr3: 148,722,369-199,307,833 CCDC50, LOC105374179, 785 more genes
    nsv3874894copy number variation1nstd102humanPathogenic GRCh37 chr3: 142,995,020-192,997,215 , GRCh38.p12 chr3: 143,276,178-193,279,426 CCDC50, RNU6-901P, 673 more genes
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