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Items: 1 to 20 of 21

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4452794copy number variation1nstd102humanPathogenic GRCh37 chr3: 165,603,872-168,796,960 , GRCh38.p12 chr3: 165,886,084-169,079,172 GOLIM4, MTND4P17, 31 more genes
    nsv3885606copy number variation1nstd102humanPathogenic GRCh37 chr3: 60,174-197,948,027 , GRCh38.p12 chr3: 18,496-198,221,156 GOLIM4, RNU4-62P, 2880 more genes
    nsv3889228copy number variation2nstd102humanPathogenic GRCh37 chr3: 61,892-197,851,986 , GRCh38.p12 chr3: 20,214-198,125,115 GOLIM4, NDUFB4, 2876 more genes
    nsv3880617copy number variation1nstd102humanPathogenic GRCh37 chr3: 61,495-197,838,262 , GRCh38.p12 chr3: 19,817-198,111,391 GOLIM4, 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 GOLIM4, LINC02614, 1469 more genes
    nsv6637156copy number variation1nstd102humanPathogenic GRCh37 chr3: 116,620,308-172,042,292 , GRCh38.p12 chr3: 116,901,461-172,324,502 GOLIM4, H1-10, 846 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 GOLIM4, LOC105374179, 785 more genes
    nsv3874894copy number variation1nstd102humanPathogenic GRCh37 chr3: 142,995,020-192,997,215 , GRCh38.p12 chr3: 143,276,178-193,279,426 GOLIM4, RNU6-901P, 673 more genes
    nsv3918066copy number variation1nstd102humanPathogenic GRCh38 chr3: 152,100,512-198,118,383 , NCBI36 chr3: 153,300,991-199,329,651 , GRCh37 chr3: 151,818,301-197,845,254 GOLIM4, LOC105374260, 696 more genes
    nsv3918149copy number variation1nstd102humanPathogenic GRCh37 chr3: 155,836,230-197,851,986 , GRCh38 chr3: 156,118,441-198,125,115 , NCBI36 chr3: 157,318,924-199,336,383 GOLIM4, LINC02031, 647 more genes
    nsv3913128copy number variation1nstd102humanPathogenic GRCh38 chr3: 156,321,878-198,113,452 , NCBI36 chr3: 157,522,361-199,324,720 , GRCh37 chr3: 156,039,667-197,840,323 GOLIM4, SNORA4, 644 more genes
    nsv3914686copy number variation1nstd102humanPathogenic NCBI36 chr3: 158,493,861-199,345,995 , GRCh37 chr3: 157,011,167-197,861,598 , GRCh38 chr3: 157,293,378-198,134,727 GOLIM4, RPL34P10, 625 more genes
    nsv3871065copy number variation1nstd102humanPathogenic GRCh37 chr3: 158,980,631-197,766,890 , GRCh38.p12 chr3: 159,262,842-198,040,019 GOLIM4, LINC02048, 599 more genes
    nsv3912173copy number variation1nstd102humanPathogenic NCBI36 chr3: 167,337,691-199,336,383 , GRCh37 chr3: 165,854,997-197,851,986 , GRCh38 chr3: 166,137,209-198,125,115 GOLIM4, LOC105374277, 540 more genes
    nsv3918784copy number variation1nstd102humanPathogenic GRCh37 chr3: 147,160,353-178,240,319 , GRCh38 chr3: 147,442,566-178,522,531 , NCBI36 chr3: 148,643,043-179,723,013 GOLIM4, LOC105374167, 394 more genes
    nsv3889215copy number variation1nstd102humanPathogenic GRCh37 chr3: 157,128,738-181,637,333 , GRCh38.p12 chr3: 157,410,949-181,919,545 GOLIM4, NAALADL2, 274 more genes
    nsv3913042copy number variation1nstd102humanPathogenic NCBI36 chr3: 166,359,093-181,330,650 , GRCh37 chr3: 164,876,399-179,847,956 , GRCh38 chr3: 165,158,611-180,130,168 GOLIM4, LOC105374211, 169 more genes
    nsv3919833copy number variation1nstd102humanPathogenic GRCh38 chr3: 158,141,556-172,788,324 , NCBI36 chr3: 159,342,039-173,988,808 , GRCh37 chr3: 157,859,345-172,506,114 GOLIM4, NMD3, 173 more genes
    nsv3914762copy number variation1nstd102humanLikely pathogenic NCBI36 chr3: 168,918,444-189,565,754 , GRCh37 chr3: 167,435,750-188,083,060 , GRCh38 chr3: 167,717,962-188,365,272 GOLIM4, ACTL6A, 325 more genes
    nsv3875281copy number variation1nstd102humanUncertain significance GRCh37 chr3: 163,595,552-168,022,596 , GRCh38.p12 chr3: 163,877,764-168,304,808 GOLIM4, LINC01322, 38 more genes
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