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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4684060copy number variation3nstd102humanPathogenic GRCh37 chr7: 74,191,613-74,191,693 , GRCh38.p12 chr7: 74,777,267-74,777,347 NCF1
    nsv7098968copy number variation1nstd102humanLikely pathogenic GRCh37 chr7: 74,188,451-74,195,125 , GRCh38.p12 chr7: 74,774,104-74,780,779 NCF1
    nsv3920720copy number variation1nstd102humanUncertain significance NCBI36 chr7: 73,779,626-73,889,366 , GRCh37.p13 chr7|NW_003871064.1: 2,256,588-2,365,544 , GRCh37.p13 chr7: 74,141,690-74,251,430 , GRCh38.p12 chr7: 74,727,352-74,836,308 NCF1, GTF2I, 3 more genes
    nsv3924467copy number variation1nstd102humanUncertain significance NCBI36 chr7: 73,779,626-73,854,093 , GRCh37.p13 chr7|NW_003871064.1: 2,256,588-2,331,052 , GRCh37.p13 chr7: 74,141,690-74,216,157 , GRCh38.p12 chr7: 74,727,352-74,801,816 NCF1, GTF2I, 3 more genes
    nsv3919826copy number variation1nstd102humanPathogenic GRCh37 chr7: 54,185-159,075,079 , GRCh38 chr7: 54,185-159,282,390 , NCBI36 chr7: 149,268-158,767,840 NCF1, RNU6-438P, 2682 more genes
    nsv3888815copy number variation1nstd102humanPathogenic GRCh37 chr7: 12,258,147-140,494,267 , GRCh38.p12 chr7: 12,218,521-140,794,467 NCF1, LOC107986817, 2014 more genes
    nsv3917508copy number variation1nstd102humanPathogenic GRCh37 chr7: 62,196,742-75,061,986 , GRCh38 chr7: 62,736,364-75,432,710 , NCBI36 chr7: 61,834,177-74,899,922 NCF1, GTF2IP4, 285 more genes
    nsv3918722copy number variation1nstd102humanPathogenic GRCh38 chr7: 71,225,344-81,735,657 , GRCh37 chr7: 70,690,330-81,364,973 , NCBI36 chr7: 70,328,266-81,202,909 NCF1, GTF2IP1, 184 more genes
    nsv3922762copy number variation1nstd102humanPathogenic GRCh37 chr7: 73,992,744-83,618,176 , GRCh38 chr7: 73,873,420-83,988,860 , NCBI36 chr7: 72,925,686-83,456,112 NCF1, PMS2P3, 142 more genes
    nsv3911276copy number variation1nstd102humanPathogenic GRCh38 chr7: 69,382,353-77,823,832 , GRCh37 chr7: 68,847,339-77,453,149 , NCBI36 chr7: 68,485,275-77,291,085 NCF1, POM121, 155 more genes
    nsv3917211copy number variation1nstd102humanPathogenic GRCh38 chr7: 74,377,395-82,031,742 , NCBI36 chr7: 73,429,661-81,498,994 , GRCh37 chr7: 73,992,744-81,661,058 NCF1, HSPB1, 123 more genes
    nsv4728820copy number variation1nstd102humanPathogenic GRCh37 chr7: 72,403,117-76,709,600 , GRCh38.p12 chr7: 72,932,579-77,080,283 NCF1, FDPSP7, 119 more genes
    nsv3902539copy number variation1nstd102humanPathogenic GRCh37 chr7: 72,456,604-76,007,380 , GRCh38.p12 chr7: 72,986,074-76,378,063 NCF1, WBSCR23, 97 more genes
    nsv3922160copy number variation1nstd102humanPathogenic NCBI36 chr7: 72,404,249-76,189,514 , GRCh38 chr7: 73,352,304-76,722,261 , GRCh37 chr7: 72,766,313-76,351,578 NCF1, PMS2P10, 88 more genes
    nsv4675200copy number variation1nstd102humanPathogenic GRCh37 chr7: 72,621,722-76,007,380 , GRCh38.p12 chr7: 73,207,682-76,378,063 NCF1, PHB1P15, 87 more genes
    nsv4349368copy number variation1nstd102humanPathogenic GRCh37 chr7: 72,744,494-76,038,818 , GRCh38.p12 chr7: 73,330,491-76,409,501 NCF1, MDH2, 83 more genes
    nsv3894940copy number variation1nstd102humanPathogenic GRCh37 chr7: 72,536,980-74,629,034 , GRCh38.p12 chr7: 73,122,656-75,175,451 NCF1, TRIM50, 53 more genes
    nsv6315397copy number variation1nstd102humanPathogenic GRCh37 chr7: 72,589,515-74,629,034 , GRCh38.p12 chr7: 73,175,475-75,175,451 NCF1, MIR10525, 52 more genes
    nsv3892254copy number variation1nstd102humanPathogenic GRCh37 chr7: 72,612,042-74,574,641 , GRCh38.p12 chr7: 73,198,002-75,158,835 NCF1, FZD9, 51 more genes
    nsv3901656copy number variation1nstd102humanPathogenic GRCh37 chr7: 72,305,671-74,196,360 , GRCh38.p12 chr7: 72,835,092-74,782,015 NCF1, ELN, 58 more genes
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