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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
    nsv4973214copy number variation1nstd200human GRCh38 chr9: 93,099,195-93,105,545 , GRCh37.p13 chr9: 95,861,477-95,867,827 CARD19
    nsv4887530inversion1nstd200human GRCh37 chr9: 90,662,371-96,951,001 , GRCh38.p12 chr9: 88,047,456-94,188,719 , MTATP6P29, 125 more genes
    nsv4611764copy number variation1nstd183human GRCh37 chr9: 95,814,750-95,917,874 , GRCh38.p12 chr9: 93,052,468-93,155,592 LOC101927993, CARD19, 2 more genes
    nsv4526483copy number variation1nstd166human GRCh37.p13 chr9: 95,858,181-95,858,256 , GRCh38.p12 chr9: 93,095,899-93,095,974 LOC101927993, CARD19
    nsv4457273copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-141,020,388 , GRCh38.p12 chr9: 203,861-138,125,936 CDRT15P14, MIR548AW, 2167 more genes
    nsv4456112copy number variation1nstd102humanUncertain significance GRCh37 chr9: 95,258,118-95,888,821 , GRCh38.p12 chr9: 92,495,836-93,126,539 IPPK, FGD3, 21 more genes
    nsv4455186copy number variation1nstd102humanPathogenic GRCh37 chr9: 71,416,475-141,020,389 , GRCh38.p12 chr9: 68,801,559-138,125,937 LOC105376327, ENG, 1304 more genes
    nsv4349215copy number variation1nstd102humanPathogenic GRCh37 chr9: 79,520,825-97,201,274 , GRCh38.p12 chr9: 76,905,909-94,438,992 SPATA31C1, LINC02893, 280 more genes
    nsv4337085sequence alteration1nstd166human GRCh37.p13 chr9: 91,988,635-138,279,888 , GRCh38.p12 chr9: 89,373,720-135,388,042 , ABCA1, 927 more genes
    nsv4190004copy number variation1nstd166human GRCh37.p13 chr9: 95,866,219-95,866,306 , GRCh38.p12 chr9: 93,103,937-93,104,024 CARD19
    nsv4189004copy number variation1nstd166human GRCh37.p13 chr9: 95,861,495-95,867,818 , GRCh38.p12 chr9: 93,099,213-93,105,536 CARD19
    nsv4184901copy number variation1nstd166human GRCh37.p13 chr9: 95,871,500-95,883,000 , GRCh38.p12 chr9: 93,109,218-93,120,718 CARD19, NINJ1
    nsv4181311copy number variation1nstd166human GRCh37.p13 chr9: 95,804,492-95,905,139 , GRCh38.p12 chr9: 93,042,210-93,142,857 LOC101927993, NINJ1, 2 more genes
    nsv4181149copy number variation1nstd166human GRCh37.p13 chr9: 95,454,728-96,167,086 , GRCh38.p12 chr9: 92,692,446-93,404,804 CARD19, SUSD3, 17 more genes
    nsv4179053copy number variation1nstd166human GRCh37.p13 chr9: 95,874,350-95,911,000 , GRCh38.p12 chr9: 93,112,068-93,148,718 NINJ1, CARD19
    nsv4177637copy number variation1nstd166human GRCh37.p13 chr9: 95,875,877-95,932,504 , GRCh38.p12 chr9: 93,113,595-93,170,222 NINJ1, CARD19
    nsv3943758copy number variation1nstd167human GRCh37 chr9: 95,858,153-95,858,186 , GRCh38.p12 chr9: 93,095,871-93,095,904 CARD19, LOC101927993
    nsv3922685copy number variation1nstd102humanPathogenic GRCh38 chr9: 88,522,292-113,687,796 , NCBI36 chr9: 90,327,027-115,489,897 , GRCh37 chr9: 91,137,207-116,450,076 MUSK, LOC105376176, 464 more genes
    nsv3922684copy number variation2nstd102humanPathogenic NCBI36 chr9: 194,193-140,193,718 , GRCh38 chr9: 193,412-138,179,445 , GRCh37 chr9: 204,193-141,073,897 TDRD7, CDK9, 2170 more genes
    nsv3922615copy number variation1nstd102humanPathogenic GRCh38 chr9: 91,596,533-97,018,746 , GRCh37 chr9: 94,358,815-99,781,028 , NCBI36 chr9: 93,398,636-98,820,849 LOC107987097, MIR4670, 137 more genes
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