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Items: 1 to 20 of 409

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097560copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr6: 107,019,871-110,266,416 , GRCh38.p12 chr6: 106,571,996-109,945,213 ZPR1P1, OSTM1, 60 more genes
    nsv7055832inversion1nstd229human GRCh38 chr6: 108,949,862-108,955,969 , GRCh37.p13 chr6: 109,271,065-109,277,172 ARMC2
    nsv7055005inversion1nstd229human GRCh38 chr6: 108,167,886-110,172,775 , GRCh37.p13 chr6: 108,489,090-110,493,978 AK9, WASF1, 34 more genes
    nsv7053812inversion1nstd229human GRCh38 chr6: 108,922,927-108,926,055 , GRCh37.p13 chr6: 109,244,130-109,247,258 ARMC2, ARMC2-AS1
    nsv7052896inversion1nstd229human GRCh38 chr6: 108,944,600-108,950,478 , GRCh37.p13 chr6: 109,265,803-109,271,681 ARMC2
    nsv7050372inversion1nstd229human GRCh38 chr6: 107,280,655-111,259,922 , GRCh37.p13 chr6: 107,601,859-111,581,125 SNORA40C, PPIL6, 77 more genes
    nsv7043260inversion1nstd229human GRCh38 chr6: 107,500,793-111,264,842 , GRCh37.p13 chr6: 107,821,997-111,586,045 ZBTB24-DT, RNU6-906P, 76 more genes
    nsv6815990copy number variation1nstd229human GRCh38 chr6: 108,989,529-108,989,570 , GRCh37.p13 chr6: 109,310,732-109,310,773 ARMC2, SESN1
    nsv6815870copy number variation1nstd229human GRCh38 chr6: 108,922,588-108,927,465 , GRCh37.p13 chr6: 109,243,791-109,248,668 ARMC2, ARMC2-AS1
    nsv6815585copy number variation1nstd229human GRCh38 chr6: 108,885,730-108,885,927 , GRCh37.p13 chr6: 109,206,933-109,207,130 ARMC2
    nsv6814404copy number variation1nstd229human GRCh38 chr6: 108,957,151-108,961,032 , GRCh37.p13 chr6: 109,278,354-109,282,235 ARMC2
    nsv6812946copy number variation1nstd229human GRCh38 chr6: 108,911,005-108,911,190 , GRCh37.p13 chr6: 109,232,208-109,232,393 ARMC2-AS1, ARMC2
    nsv6812827copy number variation1nstd229human GRCh38 chr6: 108,913,647-108,922,325 , GRCh37.p13 chr6: 109,234,850-109,243,528 ARMC2, ARMC2-AS1
    nsv6810643copy number variation1nstd229human GRCh38 chr6: 108,930,301-108,932,900 , GRCh37.p13 chr6: 109,251,504-109,254,103 ARMC2
    nsv6810132copy number variation1nstd229human GRCh38 chr6: 108,939,417-108,955,685 , GRCh37.p13 chr6: 109,260,620-109,276,888 ARMC2
    nsv6809355copy number variation1nstd229human GRCh38 chr6: 108,937,869-108,938,318 , GRCh37.p13 chr6: 109,259,072-109,259,521 ARMC2
    nsv6808735copy number variation1nstd229human GRCh38 chr6: 108,960,401-108,968,800 , GRCh37.p13 chr6: 109,281,604-109,290,003 ARMC2
    nsv6807691copy number variation1nstd229human GRCh38 chr6: 108,937,900-108,938,396 , GRCh37.p13 chr6: 109,259,103-109,259,599 ARMC2
    nsv6806338copy number variation1nstd229human GRCh38 chr6: 108,889,255-108,890,406 , GRCh37.p13 chr6: 109,210,458-109,211,609 ARMC2
    nsv6805885copy number variation1nstd229human GRCh38 chr6: 108,913,354-108,919,306 , GRCh37.p13 chr6: 109,234,557-109,240,509 ARMC2-AS1, ARMC2
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