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Items: 1 to 20 of 231

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098455copy number variation6nstd102humanUncertain significance GRCh37 chr9: 32,453,279-37,785,041 , GRCh38.p12 chr9: 32,453,281-37,785,044 TRBVAOR9-2, UBAP2, 197 more genes
    nsv7098082copy number variation1nstd102humanUncertain significance GRCh37 chr9: 34,370,797-36,276,941 , GRCh38.p12 chr9: 34,370,799-36,276,944 UNC13B, CD72, 86 more genes
    nsv7098080copy number variation1nstd102humanUncertain significance GRCh37 chr9: 32,453,279-35,068,379 , GRCh38.p12 chr9: 32,453,281-35,068,382 SUGT1P1, RNU7-36P, 110 more genes
    nsv7073398inversion1nstd229human GRCh38 chr9: 34,569,022-34,569,077 , GRCh37.p13 chr9: 34,569,020-34,569,075 LOC105376023, CNTFR, 1 more genes
    nsv7060440inversion1nstd229human GRCh38 chr9: 33,533,890-38,610,880 , GRCh37.p13 chr9: 33,533,888-38,610,877 FRMPD1, PTENP1, 182 more genes
    nsv7058978inversion1nstd229human GRCh38 chr9: 33,570,636-38,550,207 , GRCh37.p13 chr9: 33,570,634-38,550,204 TRBV29OR9-2, SPMIP6, 180 more genes
    nsv6876611copy number variation1nstd229human GRCh38 chr9: 34,574,501-34,593,500 , GRCh37.p13 chr9: 34,574,499-34,593,498 CNTFR-AS1, CNTFR
    nsv6872206copy number variation1nstd229human GRCh38 chr9: 34,559,971-34,593,240 , GRCh37.p13 chr9: 34,559,969-34,593,238 CNTFR, LOC105376023, 1 more genes
    nsv6870133copy number variation1nstd229human GRCh38 chr9: 34,043,094-35,876,103 , GRCh37.p13 chr9: 34,043,092-35,876,100 STOML2, ENHO, 85 more genes
    nsv6864935copy number variation1nstd229human GRCh38 chr9: 34,036,342-35,019,147 , GRCh37.p13 chr9: 34,036,340-35,019,144 SYF2P2, TUBB4BP2, 43 more genes
    nsv6637336copy number variation1nstd102humanUncertain significance GRCh37 chr9: 34,247,282-34,986,900 , GRCh38.p12 chr9: 34,247,284-34,986,903 ENHO, SPATA31F1, 29 more genes
    nsv6634454copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-131,603,223 , GRCh38.p12 chr9: 203,861-128,840,944 HNRNPA1P41, GAS1RR, 1868 more genes
    nsv6634409copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 1-40,036,525 , GRCh38.p12 chr9: 10,001-39,445,729 ACO1, PLIN2, 594 more genes
    nsv6560363inversion1nstd223human GRCh38 chr9: 33,533,993-38,610,852 , GRCh37.p13 chr9: 33,533,991-38,610,849 PHF24, CNTFR, 182 more genes
    nsv6449537copy number variation1nstd223human GRCh38 chr9: 34,103,197-34,805,619 , GRCh37.p13 chr9: 34,103,195-34,805,616 LOC105376023, DNAI1, 31 more genes
    nsv6315572copy number variation1nstd102humanUncertain significance GRCh38 chr9: 33,492,358-34,725,916 , GRCh37.p13 chr9: 33,492,356-34,725,913 PTENP1, KIF24, 60 more genes
    nsv6315463copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-35,903,398 , GRCh38.p12 chr9: 203,861-35,903,401 IFNA11P, RNU6-14P, 495 more genes
    nsv6315415copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-68,342,786 , GRCh38.p12 chr9: 203,861-67,920,552 LOC107987068, FAM74A7, 846 more genes
    nsv6315405copy number variation1nstd102humanUncertain significance GRCh37 chr9: 19,356,861-119,513,311 , GRCh38.p12 chr9: 19,356,863-116,751,032 RNU6-156P, GDA, 1425 more genes
    nsv6313827copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-84,155,399 , GRCh38.p12 chr9: 203,861-81,540,484 RPSAP75, ANKRD20A2P, 1008 more genes
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