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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3876139copy number variation1nstd102humanLikely benign GRCh37 chr2: 80,636,890-80,989,799 , GRCh38.p12 chr2: 80,409,765-80,762,674 CTNNA2
    nsv3885843copy number variation1nstd102humanBenign GRCh37 chr2: 79,889,616-79,897,781 , GRCh38.p12 chr2: 79,662,490-79,670,655 CTNNA2
    nsv3901876copy number variation1nstd102humanUncertain significance NCBI36 chr2: 79,948,225-80,225,680 , GRCh37 chr2: 80,094,717-80,372,169 , GRCh38 chr2: 79,867,591-80,145,043 CTNNA2
    nsv4674509copy number variation1nstd102humanUncertain significance GRCh37 chr2: 80,105,358-80,209,568 , GRCh38.p12 chr2: 79,878,232-79,982,442 CTNNA2
    nsv6636618copy number variation1nstd102humanUncertain significance GRCh37 chr2: 80,732,592-80,805,828 , GRCh38.p12 chr2: 80,505,467-80,578,703 CTNNA2
    nsv4450620copy number variation1nstd102humanUncertain significance GRCh37 chr2: 79,879,079-80,105,359 , GRCh38.p12 chr2: 79,651,953-79,878,233 CTNNA2, MIR8080
    nsv3923542copy number variation1nstd102humanUncertain significance NCBI36 chr2: 79,980,680-80,265,389 , GRCh37.p13 chr2: 80,127,172-80,411,878 , GRCh38.p12 chr2: 79,900,046-80,184,752 CTNNA2, RBM7P1
    nsv4450940copy number variation1nstd102humanUncertain significance GRCh37 chr2: 79,568,620-80,010,494 , GRCh38.p12 chr2: 79,341,494-79,783,368 CTNNA2, CTNNA2-AS1, 3 more genes
    nsv4674512copy number variation1nstd102humanUncertain significance GRCh37 chr2: 79,491,432-79,805,562 , GRCh38.p12 chr2: 79,264,306-79,578,436 CTNNA2, GNA13P1, 2 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 CTNNA2, DAZAP2P1, 2991 more genes
    nsv6634330copy number variation1nstd102humanPathogenic GRCh37 chr2: 11,504,318-111,365,996 , GRCh38.p12 chr2: 11,364,192-110,608,419 CTNNA2, 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 CTNNA2, 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 CTNNA2, RNU6-561P, 249 more genes
    nsv4451607copy number variation1nstd102humanPathogenic GRCh37 chr2: 77,907,114-87,330,965 , GRCh38.p12 chr2: 77,679,988-87,103,842 CTNNA2, REEP1, 134 more genes
    nsv4451769copy number variation1nstd102humanPathogenic GRCh37 chr2: 74,972,080-83,043,893 , GRCh38.p12 chr2: 74,744,953-82,816,769 CTNNA2, LOC105374824, 77 more genes
    nsv7137175copy number variation1nstd102humanPathogenic GRCh37 chr2: 79,740,059-80,875,994 , GRCh38.p12 chr2: 79,512,933-80,648,869 CTNNA2, GNA13P1, 8 more genes
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 CTNNA2, LOC112268439, 3737 more genes
    nsv3874648copy number variation1nstd102humanPathogenic GRCh37 chr2: 15,672-243,101,834 , GRCh38.p12 chr2: 15,672-242,157,305 CTNNA2, IGKV2OR2-10, 3737 more genes
    nsv3885544copy number variation1nstd102humanPathogenic GRCh37 chr2: 14,238-243,048,760 , GRCh38.p12 chr2: 14,238-242,106,609 CTNNA2, RNU6-674P, 3735 more genes
    nsv3882615copy number variation2nstd102humanPathogenic GRCh37 chr2: 12,771-242,783,384 , GRCh38.p12 chr2: 12,771-241,841,232 CTNNA2, MTND2P22, 3724 more genes
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