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Items: 1 to 20 of 241

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148130copy number variation1nstd102humanPathogenic GRCh37 chr8: 36,763,176-50,929,707 , GRCh38.p12 chr8: 36,905,658-50,017,147 SNTG1, RN7SL806P, 193 more genes
    nsv6633054copy number variation1nstd224human GRCh37 chr8: 42,958,833-43,791,691 , GRCh38.p12 chr8: 43,103,690-43,936,548 POMK, POTEA, 11 more genes
    nsv6633053copy number variation3nstd224human GRCh37 chr8: 42,937,273-43,791,691 , GRCh38.p12 chr8: 43,082,130-43,936,548 POMK, SNX18P27, 12 more genes
    nsv6632990copy number variation2nstd224human GRCh37 chr8: 42,939,989-43,791,691 , GRCh38.p12 chr8: 43,084,846-43,936,548 FNTA, POTEA, 12 more genes
    nsv6632633copy number variation1nstd224human GRCh37 chr8: 43,145,487-43,791,691 , GRCh38.p12 chr8: 43,290,344-43,936,548 POTEA, LOC100420534, 4 more genes
    nsv6632631copy number variation1nstd224human GRCh37 chr8: 43,008,638-43,791,691 , GRCh38.p12 chr8: 43,153,495-43,936,548 VN1R46P, RNY5P6, 10 more genes
    nsv6632564copy number variation1nstd224human GRCh37 chr8: 43,279,732-43,791,691 , GRCh38.p12 chr8: 43,424,589-43,936,548 CYP4F44P, LOC100420534, 2 more genes
    nsv6632563copy number variation4nstd224human GRCh37 chr8: 43,052,839-43,791,691 , GRCh38.p12 chr8: 43,197,696-43,936,548 VN1R46P, LOC100420534, 9 more genes
    nsv6313701copy number variation1nstd102humanUncertain significance GRCh37 chr8: 42,162,574-48,757,095 , GRCh38.p12 chr8: 42,305,056-47,844,534 RNU1-124P, LOC728587, 66 more genes
    nsv6136050copy number variation1nstd213human GRCh37 chr8: 42,670,000-43,650,001 , GRCh38.p12 chr8: 42,814,857-43,794,858 FNTA, THAP1, 18 more genes
    nsv6136049copy number variation1nstd213human GRCh37 chr8: 42,190,000-43,790,001 , GRCh38.p12 chr8: 42,332,482-43,934,858 IKBKB, SLC20A2, 29 more genes
    nsv5917461copy number variation1nstd209human GRCh38 chr8: 41,299,580-47,196,853 , GRCh37.p13 chr8: 41,157,099-48,108,476 , AFG3L2P1, 81 more genes
    nsv5200364copy number variation1nstd102humanPathogenic GRCh37 chr8: 176,814-43,396,776 , GRCh38.p12 chr8: 226,814-43,541,633 LOC100130612, XPO7, 770 more genes
    nsv4954399copy number variation1nstd200human GRCh38 chr8: 43,230,931-43,772,662 , GRCh37.p13 chr8: 43,086,074-43,627,805 , RNU6-104P, 7 more genes
    nsv4954398copy number variation1nstd200human GRCh38 chr8: 43,131,071-43,800,459 , GRCh37.p13 chr8: 42,986,214-43,655,602 , POTEA, 11 more genes
    nsv4954397copy number variation1nstd200human GRCh38 chr8: 43,129,472-43,883,107 , GRCh37.p13 chr8: 42,984,615-43,738,250 , LOC105379397, 11 more genes
    nsv4768211inversion1nstd199human GRCh37 chr8: 23,474,464-53,327,098 , GRCh38.p12 chr8: 23,616,951-52,414,538 , ADRA1A, 411 more genes
    nsv4756879inversion1nstd199human GRCh37 chr8: 23,474,453-53,323,933 , GRCh38.p12 chr8: 23,616,940-52,411,373 , ADRA1A, 411 more genes
    nsv4705892copy number variation1nstd195human GRCh37 chr8: 43,366,001-43,542,001 , GRCh38.p12 chr8: 43,510,858-43,686,858 SNX18P27, LOC105379397, 1 more genes
    nsv4679339copy number variation1nstd189human GRCh37.p13 chr8: 42,951,985-43,824,048 , GRCh38.p12 chr8: 43,096,842-43,968,905 , POMK, 12 more genes
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