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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3132270copy number variation1nstd151human GRCh37 (hg19) chr3: 185,229,309-185,232,314 , GRCh38 (hg38) chr3: 185,511,521-185,514,526 LIPH
    nsv3131096copy number variation1nstd151human GRCh37 (hg19) chr3: 185,245,269-185,307,962 , GRCh38 (hg38) chr3: 185,527,481-185,590,174 LIPH, SENP2
    nsv3131033copy number variation1nstd151human GRCh37 (hg19) chr3: 185,190,760-185,393,706 , GRCh38 (hg38) chr3: 185,472,972-185,675,918 IGF2BP2, LIPH, 3 more genes
    nsv3130850copy number variation1nstd151human GRCh37 (hg19) chr3: 182,538,045-197,765,543 , GRCh38 (hg38) chr3: 182,820,257-198,038,672 MIR922, MIR944, 199 more genes
    nsv3130763copy number variation1nstd151human GRCh37 (hg19) chr3: 185,229,309-185,252,925 , GRCh38 (hg38) chr3: 185,511,521-185,535,137 LIPH
    nsv3130568copy number variation1nstd151human GRCh37 (hg19) chr3: 185,251,356-185,316,340 , GRCh38 (hg38) chr3: 185,533,568-185,598,552 LIPH, SENP2
    nsv3130104copy number variation2nstd151human GRCh37 (hg19) chr3: 185,232,195-185,234,955 , GRCh38 (hg38) chr3: 185,514,407-185,517,167 LIPH
    nsv3128430copy number variation1nstd151human GRCh37 (hg19) chr3: 185,226,575-185,304,307 , GRCh38 (hg38) chr3: 185,508,787-185,586,519 LIPH, SENP2
    nsv3125166copy number variation1nstd151human GRCh37 (hg19) chr3: 185,190,760-185,251,472 , GRCh38 (hg38) chr3: 185,472,972-185,533,684 LIPH, TMEM41A, 1 more genes
    nsv3124205copy number variation1nstd151human GRCh37 (hg19) chr3: 185,234,852-185,245,378 , GRCh38 (hg38) chr3: 185,517,064-185,527,590 LIPH
    nsv3123792copy number variation1nstd151human GRCh37 (hg19) chr3: 185,270,208-185,344,186 , GRCh38 (hg38) chr3: 185,552,420-185,626,398 LIPH, SENP2
    nsv3122689copy number variation1nstd151human GRCh37 (hg19) chr3: 185,226,575-185,237,102 , GRCh38 (hg38) chr3: 185,508,787-185,519,314 LIPH
    nsv3121520copy number variation1nstd151human GRCh37 (hg19) chr3: 185,229,309-185,237,102 , GRCh38 (hg38) chr3: 185,511,521-185,519,314 LIPH
    nsv3121119copy number variation1nstd151human GRCh37 (hg19) chr3: 184,910,011-185,252,925 , GRCh38 (hg38) chr3: 185,192,223-185,535,137 MIR5588, EHHADH, 3 more genes
    nsv3119137copy number variation1nstd151human GRCh37 (hg19) chr3: 185,245,269-185,332,533 , GRCh38 (hg38) chr3: 185,527,481-185,614,745 LIPH, SENP2
    nsv3119120copy number variation1nstd151human GRCh37 (hg19) chr3: 185,270,208-185,347,637 , GRCh38 (hg38) chr3: 185,552,420-185,629,849 LIPH, SENP2
    nsv3118448copy number variation1nstd151human GRCh37 (hg19) chr3: 185,232,195-185,252,925 , GRCh38 (hg38) chr3: 185,514,407-185,535,137 LIPH
    nsv3109828copy number variation1nstd37humanPathogenic NCBI36 (hg18) chr3: 178,729,187-199,321,446 , GRCh37 (hg19) chr3: 177,246,493-197,837,049 , GRCh38 (hg38) chr3: 177,528,705-198,110,178 MIR922, MIR944, 230 more genes
    nsv3081496mobile element insertion2nstd144human GRCh37 (hg19) chr3: 185,262,752-185,262,752 , GRCh38 (hg38) chr3: 185,544,964-185,544,964 LIPH
    nsv3066404insertion1nstd140human GRCh37 (hg19) chr3: 185,256,533-185,256,534 , GRCh38 (hg38) chr3: 185,538,745-185,538,746 LIPH
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