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Items: 1 to 20 of 236

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099252copy number variation1nstd231human GRCh38.p12 chr1: 179,130,308-181,685,140 , GRCh37 chr1: 179,099,443-181,654,276 ABL2, CACNA1E, 48 more genes
    nsv6645740copy number variation1nstd229human GRCh38 chr1: 179,940,301-180,013,300 , GRCh37.p13 chr1: 179,909,436-179,982,435 RPSAP16, LOC101928933, 2 more genes
    nsv6645739copy number variation1nstd229human GRCh38 chr1: 179,923,701-179,937,900 , GRCh37.p13 chr1: 179,892,836-179,907,035 LOC101928933
    nsv6645738copy number variation1nstd229human GRCh38 chr1: 179,918,685-179,955,432 , GRCh37.p13 chr1: 179,887,820-179,924,567 TOR1AIP1, CEP350, 1 more genes
    nsv6645732copy number variation1nstd229human GRCh38 chr1: 179,769,936-180,207,393 , GRCh37.p13 chr1: 179,739,071-180,176,528 TOR1AIP1, TOR1AIP2, 11 more genes
    nsv6645691copy number variation1nstd229human GRCh38 chr1: 179,923,001-179,929,300 , GRCh37.p13 chr1: 179,892,136-179,898,435 LOC101928933
    nsv6645591copy number variation1nstd229human GRCh38 chr1: 179,928,007-179,937,364 , GRCh37.p13 chr1: 179,897,142-179,906,499 LOC101928933
    nsv6645215copy number variation1nstd229human GRCh38 chr1: 179,919,536-179,937,384 , GRCh37.p13 chr1: 179,888,671-179,906,519 LOC101928933, TOR1AIP1
    nsv6637124copy number variation1nstd102humanPathogenic GRCh37 chr1: 179,727,182-192,260,142 , GRCh38.p12 chr1: 179,758,047-192,291,012 LOC101928933, KIAA1614-AS1, 148 more genes
    nsv6545062inversion1nstd223human GRCh38 chr1: 179,928,883-179,929,687 , GRCh37.p13 chr1: 179,898,018-179,898,822 LOC101928933
    nsv6544237inversion1nstd223human GRCh38 chr1: 179,947,834-179,948,829 , GRCh37.p13 chr1: 179,916,969-179,917,964 LOC101928933
    nsv6543926inversion1nstd223human GRCh38 chr1: 179,928,385-179,929,666 , GRCh37.p13 chr1: 179,897,520-179,898,801 LOC101928933
    nsv6541308inversion1nstd223human GRCh38 chr1: 179,931,696-179,932,548 , GRCh37.p13 chr1: 179,900,831-179,901,683 LOC101928933
    nsv6538365inversion1nstd223human GRCh38 chr1: 178,815,320-184,820,865 , GRCh37.p13 chr1: 178,784,455-184,789,999 NPHS2, COLGALT2, 111 more genes
    nsv6327999copy number variation1nstd223human GRCh38 chr1: 179,945,223-179,950,296 , GRCh37.p13 chr1: 179,914,358-179,919,431 LOC101928933
    nsv6323342copy number variation1nstd223human GRCh38 chr1: 179,926,216-179,926,551 , GRCh37.p13 chr1: 179,895,351-179,895,686 LOC101928933
    nsv6318860copy number variation1nstd223human GRCh38 chr1: 179,769,936-180,207,393 , GRCh37.p13 chr1: 179,739,071-180,176,528 FAM163A, LOC105371634, 11 more genes
    nsv6310922copy number variation1nstd102humanUncertain significance GRCh37 chr1: 179,520,308-183,559,464 , GRCh38.p12 chr1: 179,551,173-183,590,329 NMNAT2, FAM163A, 78 more genes
    nsv6295846copy number variation1nstd186human GRCh37 chr1: 179,895,355-179,895,686 , GRCh38.p12 chr1: 179,926,220-179,926,551 LOC101928933
    nsv6290451copy number variation1nstd102humanPathogenic GRCh37 chr1: 178,522,021-190,322,133 , GRCh38.p12 chr1: 178,552,886-190,353,003 RNU7-13P, LOC105371642, 167 more genes
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