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Items: 1 to 20 of 229

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7066192inversion1nstd229human GRCh38 chr9: 94,103,087-94,103,110 , GRCh37.p13 chr9: 96,865,369-96,865,392 PTPDC1
    nsv7061653inversion1nstd229human GRCh38 chr9: 94,052,039-94,219,346 , GRCh37.p13 chr9: 96,814,321-96,981,628 LINC02603, MIRLET7D, 4 more genes
    nsv6872499copy number variation1nstd229human GRCh38 chr9: 94,062,517-94,062,689 , GRCh37.p13 chr9: 96,824,799-96,824,971 PTPDC1
    nsv6868954copy number variation1nstd229human GRCh38 chr9: 94,029,343-94,030,301 , GRCh37.p13 chr9: 96,791,625-96,792,583 PTPDC1
    nsv6858373copy number variation1nstd229human GRCh38 chr9: 94,071,401-94,076,600 , GRCh37.p13 chr9: 96,833,683-96,838,882 PTPDC1
    nsv6637944copy number variation1nstd102humanPathogenic GRCh37 chr9: 95,711,603-98,469,214 , GRCh38.p12 chr9: 92,949,321-95,706,932 MIRLET7D, MIR24-1, 60 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
    nsv6634026copy number variation3nstd224human GRCh37 chr9: 96,857,621-96,870,198 , GRCh38.p12 chr9: 94,095,339-94,107,916 PTPDC1
    nsv6567138inversion1nstd223human GRCh38 chr9: 94,067,112-94,067,672 , GRCh37.p13 chr9: 96,829,394-96,829,954 PTPDC1
    nsv6447755copy number variation1nstd223human GRCh38 chr9: 92,901,749-100,255,234 , GRCh37.p13 chr9: 95,664,031-103,017,516 EIF4BP3, VN1R51P, 162 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
    nsv6315179copy number variation1nstd102humanPathogenic GRCh37 chr9: 93,864,974-106,661,581 , GRCh38.p12 chr9: 91,102,692-103,899,300 SUGT1P4-STRA6LP, NR4A3, 255 more genes
    nsv6313900copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 71,349,994-122,603,410 , GRCh38.p12 chr9: 68,735,078-119,841,132 ABCA1, ALAD, 793 more genes
    nsv6313546copy number variation1nstd102humanPathogenic GRCh37 chr9: 353,349-141,020,389 , GRCh38.p12 chr9: 353,349-138,125,937 FAM27C, DPM2, 2166 more genes
    nsv6303028copy number variation1nstd186human GRCh37 chr9: 96,783,183-96,807,687 , GRCh38.p12 chr9: 94,020,901-94,045,405 CYCSP24, PTPDC1
    nsv6290927copy number variation1nstd102humanUncertain significance GRCh37 chr9: 96,839,257-97,047,402 , GRCh38.p12 chr9: 94,076,975-94,285,120 LOC107987099, VDAC1P11, 6 more genes
    nsv6290004inversion1nstd102humanLikely pathogenic GRCh38.p12 chr9: 12,246,100-98,797,096 , GRCh37 chr9: 12,246,100-101,559,378 ACO1, PLIN2, 1215 more genes
    nsv6137101copy number variation1nstd213human GRCh37 chr9: 96,300,000-97,030,001 , GRCh38.p12 chr9: 93,537,718-94,267,719 FAM120A, PTPDC1, 13 more genes
    nsv5919920copy number variation1nstd209human GRCh38 chr9: 94,069,126-94,069,380 , GRCh37.p13 chr9: 96,831,408-96,831,662 PTPDC1
    nsv5912494copy number variation1nstd209human GRCh38 chr9: 94,105,332-94,105,392 , GRCh37.p13 chr9: 96,867,614-96,867,674 PTPDC1
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