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Items: 1 to 20 of 324

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099187copy number variation1nstd231human GRCh38.p12 chr1: 24,354,009-27,158,528 , GRCh37 chr1: 24,680,499-27,485,019 RUNX3, CD52, 88 more genes
    nsv7044760inversion1nstd229human GRCh38 chr1: 22,155,852-26,348,296 , GRCh37.p13 chr1: 22,482,345-26,674,787 MIR4684, PDIK1L, 120 more genes
    nsv7042883inversion1nstd229human GRCh38 chr1: 24,599,662-24,683,312 , GRCh37.p13 chr1: 24,926,153-25,009,803 NCMAP, SRRM1
    nsv6647824copy number variation1nstd229human GRCh38 chr1: 24,568,401-24,574,200 , GRCh37.p13 chr1: 24,894,892-24,900,691 NCMAP
    nsv6647823copy number variation1nstd229human GRCh38 chr1: 24,563,258-24,563,347 , GRCh37.p13 chr1: 24,889,749-24,889,838 NCMAP, RPL26P8
    nsv6647816copy number variation1nstd229human GRCh38 chr1: 24,407,201-24,760,500 , GRCh37.p13 chr1: 24,733,691-25,086,991 NCMAP, RCAN3AS, 7 more genes
    nsv6647751copy number variation1nstd229human GRCh38 chr1: 24,572,901-24,579,200 , GRCh37.p13 chr1: 24,899,392-24,905,691 NCMAP
    nsv6647750copy number variation1nstd229human GRCh38 chr1: 24,564,850-24,624,255 , GRCh37.p13 chr1: 24,891,341-24,950,746 NCMAP
    nsv6647702copy number variation1nstd229human GRCh38 chr1: 24,604,187-24,608,801 , GRCh37.p13 chr1: 24,930,678-24,935,292 NCMAP
    nsv6647701copy number variation1nstd229human GRCh38 chr1: 24,602,321-24,602,590 , GRCh37.p13 chr1: 24,928,812-24,929,081 NCMAP
    nsv6647700copy number variation1nstd229human GRCh38 chr1: 24,592,914-24,597,240 , GRCh37.p13 chr1: 24,919,405-24,923,731 NCMAP
    nsv6647699copy number variation1nstd229human GRCh38 chr1: 24,569,301-24,574,300 , GRCh37.p13 chr1: 24,895,792-24,900,791 NCMAP
    nsv6647695copy number variation1nstd229human GRCh38 chr1: 24,552,404-24,556,366 , GRCh37.p13 chr1: 24,878,895-24,882,857 NCMAP, NCMAP-DT
    nsv6647299copy number variation1nstd229human GRCh38 chr1: 24,608,767-24,613,746 , GRCh37.p13 chr1: 24,935,258-24,940,237 NCMAP
    nsv6647254copy number variation1nstd229human GRCh38 chr1: 21,562,611-27,513,090 , GRCh37.p13 chr1: 21,889,104-27,839,601 RPL18AP5, LINC00339, 184 more genes
    nsv6647227copy number variation1nstd229human GRCh38 chr1: 20,848,934-27,947,465 , GRCh37.p13 chr1: 21,175,427-28,273,976 RPL17P9, ALPL, 218 more genes
    nsv6626009copy number variation1nstd224human GRCh37 chr1: 24,906,711-24,932,733 , GRCh38.p12 chr1: 24,580,220-24,606,242 NCMAP
    nsv6553329inversion1nstd223human GRCh38 chr1: 24,598,684-24,599,232 , GRCh37.p13 chr1: 24,925,175-24,925,723 NCMAP
    nsv6548637inversion1nstd223human GRCh38 chr1: 24,598,623-24,599,180 , GRCh37.p13 chr1: 24,925,114-24,925,671 NCMAP
    nsv6537367inversion1nstd223human GRCh38 chr1: 24,593,466-24,593,986 , GRCh37.p13 chr1: 24,919,957-24,920,477 NCMAP
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