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Items: 1 to 20 of 94

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097266copy number variation1nstd102humanPathogenic GRCh37 chr5: 167,849,013-169,661,202 , GRCh38.p12 chr5: 168,422,008-170,234,198 FBLL1, RNU6-477P, 25 more genes
    nsv6796477copy number variation1nstd229human GRCh38 chr5: 168,531,878-169,361,925 , GRCh37.p13 chr5: 167,958,883-168,788,929 MIR103A1, MIR218-2, 11 more genes
    nsv6796421copy number variation1nstd229human GRCh38 chr5: 169,030,935-169,032,568 , GRCh37.p13 chr5: 168,457,940-168,459,573 SLIT3-AS1, SLIT3
    nsv6793396copy number variation1nstd229human GRCh38 chr5: 169,001,968-169,014,888 , GRCh37.p13 chr5: 168,428,973-168,441,893 SLIT3, SLIT3-AS1
    nsv6793362copy number variation1nstd229human GRCh38 chr5: 169,015,951-169,015,988 , GRCh37.p13 chr5: 168,442,956-168,442,993 SLIT3-AS1, SLIT3
    nsv6792360copy number variation1nstd229human GRCh38 chr5: 169,005,418-169,012,176 , GRCh37.p13 chr5: 168,432,423-168,439,181 SLIT3, SLIT3-AS1
    nsv6636891copy number variation1nstd102humanPathogenic GRCh37 chr5: 150,535,183-172,906,793 , GRCh38.p12 chr5: 151,155,622-173,479,790 EFCAB9, LOC112267936, 287 more genes
    nsv6315448copy number variation1nstd102humanPathogenic GRCh37 chr5: 149,010,383-180,719,789 , GRCh38.p12 chr5: 149,630,820-181,292,788 GRM6, MIR1229, 554 more genes
    nsv6256451mobile element insertion1nstd215human GRCh38 chr5: 169,035,629-169,035,629 , GRCh37.p13 chr5: 168,462,634-168,462,634 SLIT3-AS1, SLIT3
    nsv6136093copy number variation1nstd213human GRCh37 chr5: 166,260,000-169,230,001 , GRCh38.p12 chr5: 166,832,995-169,802,997 DOCK2, RARS1, 26 more genes
    nsv6136090copy number variation1nstd213human GRCh37 chr5: 161,030,000-172,600,001 , GRCh38.p12 chr5: 161,602,994-173,172,998 BNIP1, CCNG1, 130 more genes
    nsv6135205copy number variation1nstd213human GRCh37 chr5: 91,690,000-180,740,001 , GRCh38.p12 chr5: 92,354,293-181,313,000 ADRA1B, ASS1P10, 1378 more genes
    nsv4949201copy number variation1nstd200human GRCh38 chr5: 169,024,902-169,034,488 , GRCh37.p13 chr5: 168,451,907-168,461,493 SLIT3, SLIT3-AS1
    nsv4939835copy number variation1nstd200human GRCh38 chr5: 169,016,224-169,021,092 , GRCh37.p13 chr5: 168,443,229-168,448,097 SLIT3-AS1, SLIT3
    nsv4824388copy number variation1nstd200human GRCh37 chr5: 168,451,907-168,461,493 , GRCh38.p12 chr5: 169,024,902-169,034,488 SLIT3, SLIT3-AS1
    nsv4729368copy number variation1nstd102humanLikely pathogenic GRCh37 chr5: 166,378,793-170,174,830 , GRCh38.p12 chr5: 166,951,788-170,747,826 DOCK2, FOXI1, 38 more genes
    nsv4674945copy number variation1nstd102humanPathogenic GRCh37 chr5: 156,347,980-169,959,880 , GRCh38.p12 chr5: 156,920,969-170,532,876 LINC02227, LINC01932, 146 more genes
    nsv4578263copy number variation1nstd102humanPathogenic GRCh37 chr5: 166,420,934-173,324,844 , GRCh38.p12 chr5: 166,993,929-173,897,841 LINC01187, TENM2-AS1, 112 more genes
    nsv4455586copy number variation1nstd102humanPathogenic GRCh37 chr5: 156,597,181-171,166,353 , GRCh38.p12 chr5: 157,170,170-171,739,349 LOC105377677, GABRA6, 164 more genes
    nsv4121566copy number variation1nstd166human GRCh37.p13 chr5: 168,462,089-168,462,447 , GRCh38.p12 chr5: 169,035,084-169,035,442 SLIT3, SLIT3-AS1
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