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Items: 1 to 20 of 176

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7072647inversion1nstd229human GRCh38 chr17: 59,963,909-59,967,144 , GRCh37.p13 chr17: 58,041,270-58,044,505 TBC1D3P1-DHX40P1, RNFT1, 1 more genes
    nsv7072318inversion1nstd229human GRCh38 chr17: 59,590,973-59,987,143 , GRCh37.p13 chr17: 57,668,334-58,064,504 TUBD1, MIR21, 12 more genes
    nsv7070986inversion1nstd229human GRCh38 chr17: 59,331,393-62,738,993 , GRCh37.p13 chr17: 57,408,754-60,816,354 MIR21, LINC01476, 83 more genes
    nsv7069026inversion1nstd229human GRCh38 chr17: 59,950,985-59,951,128 , GRCh37.p13 chr17: 58,028,346-58,028,489 RPS6KB1, RNFT1
    nsv7064930inversion1nstd229human GRCh38 chr17: 59,936,067-60,035,897 , GRCh37.p13 chr17: 58,013,428-58,113,258 TBC1D3P1, DHX40P1, 5 more genes
    nsv7063173inversion1nstd229human GRCh38 chr17: 59,885,051-60,090,045 , GRCh37.p13 chr17: 57,962,412-58,167,406 DHX40P1, RPS29P21, 13 more genes
    nsv7062720inversion1nstd229human GRCh38 chr17: 59,931,864-60,086,494 , GRCh37.p13 chr17: 58,009,225-58,163,855 DHX40P1, TBC1D3P1, 10 more genes
    nsv7062565inversion1nstd229human GRCh38 chr17: 59,963,907-59,971,617 , GRCh37.p13 chr17: 58,041,268-58,048,978 RNFT1, RNFT1-DT, 1 more genes
    nsv7062151inversion1nstd229human GRCh38 chr17: 58,705,434-61,610,111 , GRCh37.p13 chr17: 56,782,795-59,687,472 RNU4-13P, LOC105371850, 74 more genes
    nsv6978214copy number variation1nstd229human GRCh38 chr17: 59,960,920-59,968,013 , GRCh37.p13 chr17: 58,038,281-58,045,374 RNFT1, TBC1D3P1-DHX40P1, 1 more genes
    nsv6577246inversion1nstd223human GRCh38 chr17: 59,600,626-59,987,959 , GRCh37.p13 chr17: 57,677,987-58,065,320 PTRH2, RPS6KB1, 12 more genes
    nsv6532945copy number variation1nstd223human GRCh38 chr17: 59,949,501-59,950,500 , GRCh37.p13 chr17: 58,026,862-58,027,861 RPS6KB1, RNFT1
    nsv6527867copy number variation1nstd223human GRCh38 chr17: 59,951,166-59,951,705 , GRCh37.p13 chr17: 58,028,527-58,029,066 RNFT1
    nsv6517292copy number variation1nstd223human GRCh38 chr17: 59,949,101-59,950,700 , GRCh37.p13 chr17: 58,026,462-58,028,061 RNFT1, RPS6KB1
    nsv6310393copy number variation1nstd102humanUncertain significance GRCh37 chr17: 54,671,585-59,938,900 , GRCh38.p12 chr17: 56,594,224-61,861,539 RNF43, LOC107985048, 132 more genes
    nsv6291649copy number variation1nstd102humanPathogenic GRCh37 chr17: 57,605,300-59,389,547 , GRCh38.p12 chr17: 59,527,939-61,312,186 RNU4-13P, PTRH2, 48 more genes
    nsv6133316copy number variation1nstd213human GRCh37 chr17: 53,930,000-62,410,001 , GRCh38.p12 chr17: 55,852,639-64,332,641 CA4, CD79B, 208 more genes
    nsv6105184inversion1nstd212human GRCh38 chr17: 59,600,626-59,987,963 , GRCh37.p13 chr17: 57,677,987-58,065,324 CLTC, RPS6KB1, 12 more genes
    nsv6088488insertion1nstd212human GRCh38 chr17: 59,951,207-59,951,207 , GRCh37.p13 chr17: 58,028,568-58,028,568 RNFT1
    nsv5661845insertion1nstd207human GRCh38 chr17: 59,959,024-59,959,024 , GRCh37.p13 chr17: 58,036,385-58,036,385 RNFT1
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