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Items: 1 to 20 of 47

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4683559copy number variation1nstd102humanPathogenic GRCh37 chr9: 97,401,403-97,401,612 , GRCh38.p12 chr9: 94,639,121-94,639,330 FBP1
    nsv4685729copy number variation1nstd102humanPathogenic GRCh37 chr9: 97,401,423-97,401,593 , GRCh38.p12 chr9: 94,639,141-94,639,311 FBP1
    nsv7137112copy number variation1nstd102humanPathogenic GRCh37 chr9: 97,401,423-97,401,592 , GRCh38.p12 chr9: 94,639,141-94,639,310 FBP1
    nsv7148048copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 97,401,422-97,401,800 , GRCh38.p12 chr9: 94,639,140-94,639,518 FBP1
    nsv6312945copy number variation1nstd102humanUncertain significance GRCh37 chr9: 97,365,663-97,401,592 , GRCh38.p12 chr9: 94,603,381-94,639,310 FBP1
    nsv6313294copy number variation1nstd102humanUncertain significance GRCh37 chr9: 97,365,663-97,372,363 , GRCh38.p12 chr9: 94,603,381-94,610,081 FBP1
    nsv6638083insertion1nstd102humanUncertain significance GRCh38 chr9: 94,625,120-94,625,120 , GRCh37 chr9: 97,387,402-97,387,402 FBP1
    nsv3893407copy number variation1nstd102humanLikely benign GRCh37 chr9: 97,290,466-97,419,146 , GRCh38.p12 chr9: 94,528,184-94,656,864 FBP1, FBP2, 1 more genes
    nsv6637673copy number variation1nstd102humanUncertain significance GRCh37 chr9: 97,281,155-97,456,120 , GRCh38.p12 chr9: 94,518,873-94,693,838 FBP1, PCAT7, 2 more genes
    nsv6315179copy number variation1nstd102humanPathogenic GRCh37 chr9: 93,864,974-106,661,581 , GRCh38.p12 chr9: 91,102,692-103,899,300 FBP1, SUGT1P4-STRA6LP, 255 more genes
    nsv4684256copy number variation1nstd102humanPathogenic GRCh37 chr9: 96,126,075-108,535,272 , GRCh38.p12 chr9: 93,363,793-105,772,991 FBP1, RPS26P37, 238 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 FBP1, LOC107987097, 137 more genes
    nsv4676103copy number variation1nstd102humanPathogenic NCBI36 chr9: 95,946,863-99,986,314 , GRCh37.p13 chr9: 96,907,042-100,946,493 , GRCh38.p12 chr9: 94,144,760-98,184,211 FBP1, MIR3074, 108 more genes
    nsv3902497copy number variation1nstd102humanPathogenic GRCh37 chr9: 96,732,332-100,175,689 , GRCh38.p12 chr9: 93,970,050-97,413,407 FBP1, MIR24-1, 95 more genes
    nsv6637944copy number variation1nstd102humanPathogenic GRCh37 chr9: 95,711,603-98,469,214 , GRCh38.p12 chr9: 92,949,321-95,706,932 FBP1, MIRLET7D, 60 more genes
    nsv3904553copy number variation1nstd102humanPathogenic GRCh37 chr9: 97,355,862-99,805,480 , GRCh38.p12 chr9: 94,593,580-97,043,198 FBP1, LOC105376157, 55 more genes
    nsv3912247copy number variation1nstd102humanPathogenic NCBI36 chr9: 2,934-140,273,252 , GRCh37.p13 chr9: 12,934-141,153,431 , GRCh38.p12 chr9: 12,934-138,262,981 FBP1, ALOX15P2, 2184 more genes
    nsv3890420copy number variation1nstd102humanPathogenic GRCh37 chr9: 10,590-141,122,247 , GRCh38.p12 chr9: 10,590-138,231,797 FBP1, TBC1D13, 2183 more genes
    nsv3905118copy number variation1nstd102humanPathogenic GRCh37 chr9: 10,590-141,114,095 , GRCh38.p12 chr9: 10,590-138,223,645 FBP1, MIR219A2, 2183 more genes
    nsv3891842copy number variation1nstd102humanPathogenic GRCh37 chr9: 10,590-141,107,672 , GRCh38.p12 chr9: 10,590-138,217,222 FBP1, OR13C1P, 2183 more genes
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