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Items: 1 to 20 of 188

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5922760copy number variation1nstd209human GRCh38 chr7: 5,058,166-5,059,411 , GRCh37.p13 chr7: 5,097,797-5,099,042 RBAK, RBAK-RBAKDN
    nsv5922417copy number variation1nstd209human GRCh38 chr7: 5,059,877-5,059,960 , GRCh37.p13 chr7: 5,099,508-5,099,591 RBAK-RBAKDN, RBAK
    nsv5570348copy number variation1nstd207human GRCh38 chr7: 5,048,861-5,048,984 , GRCh37.p13 chr7: 5,088,492-5,088,615 RBAK, RBAK-RBAKDN
    nsv5562206sequence alteration1nstd206human GRCh38 chr7: 4,983,711-5,730,820 , GRCh37.p13 chr7: 5,023,342-5,770,451 , FSCN1, 21 more genes
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv4953275copy number variation1nstd200human GRCh38 chr7: 4,827,430-5,111,612 , GRCh37.p13 chr7: 4,867,061-5,151,243 RBAK, LOC105375134, 9 more genes
    nsv4828706copy number variation1nstd200human GRCh37 chr7: 4,867,061-5,151,243 , GRCh38.p12 chr7: 4,827,430-5,111,612 LOC105375134, RBAK, 9 more genes
    nsv4729642copy number variation1nstd102humanUncertain significance GRCh37 chr7: 4,457,599-5,138,409 , GRCh38.p12 chr7: 4,417,968-5,098,778 LOC105375134, MIR4656, 15 more genes
    nsv4729297copy number variation1nstd102humanUncertain significance GRCh37 chr7: 4,733,073-5,157,165 , GRCh38.p12 chr7: 4,693,442-5,117,534 RBAKDN, RNF216P1, 13 more genes
    nsv4714659copy number variation1nstd195human GRCh37 chr7: 5,096,701-5,110,201 , GRCh38.p12 chr7: 5,057,070-5,070,570 RBAK, RBAKDN, 1 more genes
    nsv4675935copy number variation1nstd102humanLikely benign GRCh37 chr7: 5,066,179-5,203,597 , GRCh38.p12 chr7: 5,026,548-5,163,966 RBAK, RBAKDN, 5 more genes
    nsv4675817copy number variation1nstd102humanPathogenic GRCh37 chr7: 1,648,373-10,627,513 , GRCh38.p12 chr7: 1,608,737-10,587,886 TTYH3, UNC93B2, 150 more genes
    nsv4606076copy number variation1nstd183human GRCh37 chr7: 5,066,193-5,205,944 , GRCh38.p12 chr7: 5,026,562-5,166,313 RBAK, RBAKDN, 5 more genes
    nsv4554029insertion1nstd166human GRCh37.p13 chr7: 5,102,275-5,102,275 , GRCh38.p12 chr7: 5,062,644-5,062,644 RBAK, RBAK-RBAKDN
    nsv4456827copy number variation1nstd102humanPathogenic GRCh37 chr7: 43,376-19,520,619 , GRCh38.p12 chr7: 43,376-19,480,996 MIR6836, EEF1A1P26, 277 more genes
    nsv4455091copy number variation1nstd102humanPathogenic GRCh37 chr7: 10,365-159,119,707 , GRCh38.p12 chr7: 10,365-159,327,017 RPL23AP51, FLJ40288, 2684 more genes
    nsv4407155copy number variation1nstd174human GRCh37 chr7: 5,068,892-5,086,142 , GRCh38.p12 chr7: 5,029,261-5,046,511 RBAK, LOC105375134, 2 more genes
    nsv4398367copy number variation1nstd174human GRCh37 chr7: 4,802,287-5,138,409 , GRCh38.p12 chr7: 4,762,656-5,098,778 MIR4656, RBAK-RBAKDN, 12 more genes
    nsv4395302copy number variation1nstd174human GRCh37 chr7: 5,036,761-5,114,089 , GRCh38.p12 chr7: 4,997,130-5,074,458 RBAK, RBAKDN, 4 more genes
    nsv4143759copy number variation1nstd166human GRCh37.p13 chr7: 5,107,867-5,110,824 , GRCh38.p12 chr7: 5,068,236-5,071,193 RBAKDN, RBAK, 1 more genes
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