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Items: 1 to 20 of 147

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5974071inversion1nstd209human GRCh37.p13 chr7|NW_003871064.1: 478,880-2,946,547 , GRCh38 chr7: 72,949,644-75,417,311 , CLDN4, 79 more genes
    nsv5918891copy number variation1nstd209human GRCh38 chr7: 71,592,506-75,175,408 , GRCh37.p13 chr7|NW_003871064.1: 1-2,704,644 , GRCh37.p13 chr7: 71,935,722-74,527,751 , SPDYE10, 78 more genes
    nsv5666565inversion1nstd207human GRCh38 chr7: 73,113,990-75,217,887 , GRCh37.p13 chr7|NW_003871064.1: 643,226-2,747,123 , CLDN4, 57 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
    nsv5481619copy number variation1nstd206human GRCh38 chr7: 75,154,486-75,155,341 , GRCh37.p13 chr7|NW_003871064.1: 2,683,722-2,684,577 NCF1C
    nsv5220489copy number variation1nstd204human GRCh38.p13 chr7: 75,151,901-75,155,700 , GRCh37.p13 chr7|NW_003871064.1: 2,681,137-2,684,936 NCF1C
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv4763531inversion1nstd199human GRCh37 chr7: 66,769,373-102,019,339 , GRCh38.p12 chr7: 67,304,386-102,378,892 , ACHE, 578 more genes
    nsv4730256inversion12nstd198human GRCh38 chr7: 72,909,603-75,903,316 , GRCh37.p13 chr7|NW_003871064.1: 438,839-3,432,552 , CLDN4, 86 more genes
    nsv4728820copy number variation1nstd102humanPathogenic GRCh37 chr7: 72,403,117-76,709,600 , GRCh38.p12 chr7: 72,932,579-77,080,283 FDPSP7, LOC105375352, 119 more genes
    nsv4675200copy number variation1nstd102humanPathogenic GRCh37 chr7: 72,621,722-76,007,380 , GRCh38.p12 chr7: 73,207,682-76,378,063 PHB1P15, FKBP6P2, 87 more genes
    nsv4662063copy number variation1nstd186human GRCh37 chr7: 74,563,528-75,030,992 , GRCh38.p12 chr7: 75,147,722-75,401,709 PMS2P2, SPDYE13, 12 more genes
    nsv4615922copy number variation2nstd183human GRCh37 chr7: 74,563,528-75,030,992 , GRCh38.p12 chr7: 75,147,722-75,401,709 GTF2IRD2B, SPDYE13, 12 more genes
    nsv4613975copy number variation1nstd183human GRCh37 chr7: 74,582,294-74,582,339 , GRCh38.p12 chr7: 75,166,489-75,166,534 NCF1C
    nsv4456986copy number variation1nstd102humanPathogenic GRCh37 chr7: 73,799,886-75,388,031 , GRCh38.p12 chr7: 74,385,556-75,758,713 SPDYE13, MIR10525, 33 more genes
    nsv4456466copy number variation1nstd102humanUncertain significance GRCh37 chr7: 74,165,273-74,628,840 , GRCh38.p12 chr7: 74,750,941-75,175,451 RCC1L, GTF2IRD2, 9 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
    nsv4375613copy number variation1nstd173human GRCh37 chr7: 74,483,848-74,621,643 , GRCh38.p12 chr7: 75,068,035-75,175,451 NCF1C, RCC1L, 1 more genes
    nsv4352523inversion1nstd102humanPathogenic GRCh37 chr7: 20,954,043-114,556,605 , GRCh38.p12 chr7: 20,914,424-114,916,550 ACHE, ADCY1, 1532 more genes
    nsv4349368copy number variation1nstd102humanPathogenic GRCh37 chr7: 72,744,494-76,038,818 , GRCh38.p12 chr7: 73,330,491-76,409,501 MDH2, BUD23, 83 more genes
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