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Items: 1 to 20 of 293

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148229copy number variation1nstd102humanPathogenic GRCh38 chr4: 2,904,667-42,963,232 , GRCh37.p13 chr4: 2,906,394-42,965,249 LINC01587, RN7SKP82, 509 more genes
    nsv7148161copy number variation1nstd102humanPathogenic GRCh38 chr4: 1-49,062,177 , GRCh37.p13 chr4: 507,005-49,064,194 SLIRPP2, STIM2-AS1, 659 more genes
    nsv7148157copy number variation1nstd102humanPathogenic GRCh38 chr4: 85,624-57,073,230 , GRCh37.p13 chr4: 507,005-57,939,396 OR7E84P, FAM193A, 764 more genes
    nsv7137196copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,345-34,512,694 , GRCh38.p12 chr4: 68,453-34,511,072 ECM1P2, LOC105378240, 482 more genes
    nsv7057381inversion1nstd229human GRCh38 chr4: 10,020,130-10,761,825 , GRCh37.p13 chr4: 10,021,754-10,763,449 LOC100287951, LOC100422638, 16 more genes
    nsv7056884inversion1nstd229human GRCh38 chr4: 10,029,985-10,684,733 , GRCh37.p13 chr4: 10,031,609-10,686,357 SLC2A9, WDR1, 15 more genes
    nsv7053771inversion1nstd229human GRCh38 chr4: 10,327,261-10,661,981 , GRCh37.p13 chr4: 10,328,885-10,663,605 CLNK, LOC105374482, 6 more genes
    nsv7052893inversion1nstd229human GRCh38 chr4: 10,065,315-10,781,846 , GRCh37.p13 chr4: 10,066,939-10,783,470 WDR1, MIR3138, 15 more genes
    nsv7050522inversion1nstd229human GRCh38 chr4: 4,174,346-12,367,773 , GRCh37.p13 chr4: 4,176,073-12,369,397 USP17L29, MIR4274, 165 more genes
    nsv7048608inversion1nstd229human GRCh38 chr4: 9,801,923-10,517,062 , GRCh37.p13 chr4: 9,803,547-10,518,686 LOC100129344, SLC2A9-AS1, 14 more genes
    nsv6736426copy number variation1nstd229human GRCh38 chr4: 10,034,439-10,748,726 , GRCh37.p13 chr4: 10,036,063-10,750,350 LOC100130072, RAF1P1, 16 more genes
    nsv6736202copy number variation1nstd229human GRCh38 chr4: 9,649,300-10,719,450 , GRCh37.p13 chr4: 9,650,924-10,721,074 SLC2A9-AS1, LOC100129344, 23 more genes
    nsv6736026copy number variation1nstd229human GRCh38 chr4: 9,866,503-11,313,473 , GRCh37.p13 chr4: 9,868,127-11,315,097 ZNF518B, CLNK, 19 more genes
    nsv6735943copy number variation1nstd229human GRCh38 chr4: 10,050,968-10,797,198 , GRCh37.p13 chr4: 10,052,592-10,798,822 CLNK, LOC107986260, 16 more genes
    nsv6733622copy number variation1nstd229human GRCh38 chr4: 10,434,348-10,442,632 , GRCh37.p13 chr4: 10,435,972-10,444,256 ZNF518B
    nsv6733616copy number variation1nstd229human GRCh38 chr4: 10,110,897-10,540,450 , GRCh37.p13 chr4: 10,112,521-10,542,074 LOC100422639, ZNF518B, 11 more genes
    nsv6732142copy number variation1nstd229human GRCh38 chr4: 9,844,466-10,818,272 , GRCh37.p13 chr4: 9,846,090-10,819,896 LOC100129344, LOC105374482, 18 more genes
    nsv6724023copy number variation1nstd229human GRCh38 chr4: 10,438,089-10,438,467 , GRCh37.p13 chr4: 10,439,713-10,440,091 ZNF518B
    nsv6723208copy number variation1nstd229human GRCh38 chr4: 5,355,032-14,502,279 , GRCh37.p13 chr4: 5,356,759-14,503,903 OR7E86P, LINC02447, 164 more genes
    nsv6723107copy number variation1nstd229human GRCh38 chr4: 9,680,613-10,868,191 , GRCh37.p13 chr4: 9,682,237-10,869,815 LINC02498, LOC105374479, 24 more genes
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