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Items: 1 to 20 of 144

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5916810copy number variation1nstd209human GRCh38 chr9: 93,010,609-93,010,677 , GRCh37.p13 chr9: 95,772,891-95,772,959 FGD3, LOC101927954
    nsv5641725insertion1nstd207human GRCh38 chr9: 93,010,609-93,010,609 , GRCh37.p13 chr9: 95,772,891-95,772,891 LOC101927954, FGD3
    nsv5640218insertion1nstd207human GRCh38 chr9: 93,010,665-93,010,665 , GRCh37.p13 chr9: 95,772,947-95,772,947 FGD3, LOC101927954
    nsv5601095copy number variation1nstd207human GRCh38 chr9: 93,010,620-93,010,690 , GRCh37.p13 chr9: 95,772,902-95,772,972 LOC101927954, FGD3
    nsv5491934copy number variation1nstd206human GRCh38 chr9: 93,010,487-93,010,615 , GRCh37.p13 chr9: 95,772,769-95,772,897 LOC101927954, FGD3
    nsv4974713copy number variation1nstd200human GRCh38 chr9: 93,009,140-93,012,191 , GRCh37.p13 chr9: 95,771,422-95,774,473 LOC101927954, FGD3
    nsv4887530inversion1nstd200human GRCh37 chr9: 90,662,371-96,951,001 , GRCh38.p12 chr9: 88,047,456-94,188,719 , MTATP6P29, 125 more genes
    nsv4745955copy number variation1nstd199human GRCh37 chr9: 95,772,913-95,772,982 , GRCh38.p12 chr9: 93,010,631-93,010,700 FGD3, LOC101927954
    nsv4484303mobile element insertion1nstd166human GRCh37.p13 chr9: 95,768,513-95,768,513 , GRCh38.p12 chr9: 93,006,231-93,006,231 FGD3, LOC101927954
    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
    nsv4415571copy number variation1nstd174human GRCh37 chr9: 95,772,702-95,773,175 , GRCh38.p12 chr9: 93,010,420-93,010,893 LOC101927954, FGD3
    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
    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
    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
    nsv3921598copy number variation1nstd102humanPathogenic GRCh38 chr9: 203,861-138,125,937 , NCBI36 chr9: 193,861-140,140,210 , GRCh37 chr9: 203,861-141,020,389 PGAP4, ECPAS, 2167 more genes
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