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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3882112copy number variation1nstd102humanBenign GRCh37 chr2: 75,374,043-75,389,492 , GRCh38.p12 chr2: 75,146,917-75,162,366 TACR1, LOC105374811
    nsv3871110copy number variation1nstd102humanBenign GRCh37 chr2: 75,363,423-75,374,043 , GRCh38.p12 chr2: 75,136,297-75,146,917 TACR1, LOC105374811
    nsv3882107copy number variation1nstd102humanBenign GRCh37 chr2: 75,170,336-75,314,020 , GRCh38.p12 chr2: 74,943,209-75,086,893 TACR1, LOC105374809, 1 more genes
    nsv3889532copy number variation1nstd102humanBenign GRCh37 chr2: 75,185,398-75,314,020 , GRCh38.p12 chr2: 74,958,271-75,086,893 TACR1, POLE4, 1 more genes
    nsv3910630copy number variation1nstd102humanPathogenic NCBI36 chr2: 50,739,936-242,751,149 , GRCh37.p13 chr2: 50,886,432-243,102,476 , GRCh38.p12 chr2: 50,659,294-242,160,331 TACR1, DAZAP2P1, 2991 more genes
    nsv6634330copy number variation1nstd102humanPathogenic GRCh37 chr2: 11,504,318-111,365,996 , GRCh38.p12 chr2: 11,364,192-110,608,419 TACR1, CYP1B1-AS1, 1649 more genes
    nsv3877742copy number variation1nstd102humanPathogenic GRCh37 chr2: 74,365,484-89,129,064 , GRCh38.p12 chr2: 74,138,357-88,829,551 TACR1, RNU6-561P, 253 more genes
    nsv3886532copy number variation1nstd102humanPathogenic GRCh37 chr2: 74,527,522-89,125,488 , GRCh38.p12 chr2: 74,300,395-88,825,975 TACR1, RNU6-561P, 249 more genes
    nsv4451769copy number variation1nstd102humanPathogenic GRCh37 chr2: 74,972,080-83,043,893 , GRCh38.p12 chr2: 74,744,953-82,816,769 TACR1, LOC105374824, 77 more genes
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 TACR1, LOC112268439, 3737 more genes
    nsv3874648copy number variation1nstd102humanPathogenic GRCh37 chr2: 15,672-243,101,834 , GRCh38.p12 chr2: 15,672-242,157,305 TACR1, IGKV2OR2-10, 3737 more genes
    nsv3885544copy number variation1nstd102humanPathogenic GRCh37 chr2: 14,238-243,048,760 , GRCh38.p12 chr2: 14,238-242,106,609 TACR1, RNU6-674P, 3735 more genes
    nsv3882615copy number variation2nstd102humanPathogenic GRCh37 chr2: 12,771-242,783,384 , GRCh38.p12 chr2: 12,771-241,841,232 TACR1, MTND2P22, 3724 more genes
    nsv3916821copy number variation1nstd102humanPathogenic NCBI36 chr2: 47,701,031-86,783,356 , GRCh37.p13 chr2: 47,847,527-86,929,845 , GRCh38.p12 chr2: 47,620,388-86,702,722 TACR1, NAGK, 595 more genes
    nsv3900298copy number variation1nstd102humanPathogenic GRCh37 chr2: 58,506,654-83,814,086 , GRCh38 chr2: 58,279,519-83,586,962 , NCBI36 chr2: 58,360,158-83,667,597 TACR1, MIR1285-2, 404 more genes
    nsv3883931copy number variation1nstd102humanPathogenic GRCh37 chr2: 63,671,346-85,698,002 , GRCh38.p12 chr2: 63,444,212-85,470,879 TACR1, LINC01888, 367 more genes
    nsv6314726copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 40,607,042-146,902,764 , GRCh38.p12 chr2: 40,379,902-146,145,196 TACR1, ACTG2, 1713 more genes
    nsv3909450copy number variation1nstd102humanLikely pathogenic NCBI36 chr2: 74,456,414-75,598,154 , GRCh37 chr2: 74,602,906-75,744,646 , GRCh38 chr2: 74,375,779-75,517,520 TACR1, AUP1, 39 more genes
    nsv3881030copy number variation1nstd102humanBenign GRCh37 chr2: 75,050,732-75,307,296 , GRCh38.p12 chr2: 74,823,605-75,080,169 TACR1, HK2, 4 more genes
    nsv3903805copy number variation1nstd102humanBenign GRCh37 chr2: 7,635,254-88,005,418 , NCBI36 chr2: 7,552,705-87,786,533 , GRCh38 chr2: 7,495,123-87,705,899 TACR1, LOC101927723, 1246 more genes
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