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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5903830copy number variation1nstd209human GRCh38 chr2: 183,124,916-183,125,472 , GRCh37.p13 chr2: 183,989,644-183,990,200 NUP35
    nsv5560580sequence alteration1nstd206human GRCh38 chr2: 151,447,581-231,256,535 , GRCh37.p13 chr2: 152,304,095-232,121,248 , ATIC, 1163 more genes
    nsv5452774copy number variation1nstd206human GRCh38 chr2: 183,124,918-183,125,473 , GRCh37.p13 chr2: 183,989,646-183,990,201 NUP35
    nsv5444727copy number variation1nstd206human GRCh38 chr2: 183,116,952-183,122,117 , GRCh37.p13 chr2: 183,981,680-183,986,845 NUP35
    nsv5441981copy number variation1nstd206human GRCh38 chr2: 183,114,883-183,116,221 , GRCh37.p13 chr2: 183,979,611-183,980,949 NUP35
    nsv5296345copy number variation1nstd204human GRCh38.p13 chr2: 183,124,908-183,125,476 , GRCh37.p13 chr2: 183,989,636-183,990,204 NUP35
    nsv5287852copy number variation1nstd204human GRCh38.p13 chr2: 182,396,620-186,452,557 , GRCh37.p13 chr2: 183,261,347-187,317,284 , LINC01473, 36 more genes
    nsv5207655copy number variation1nstd204human GRCh38.p13 chr2: 182,398,101-183,929,800 , GRCh37.p13 chr2: 183,262,828-184,794,527 , DNAJC10, 11 more genes
    nsv5204074copy number variation1nstd204human GRCh38.p13 chr2: 183,145,800-183,146,999 , GRCh37.p13 chr2: 184,010,528-184,011,727 NUP35
    nsv5201893copy number variation1nstd204human GRCh38.p13 chr2: 183,085,772-183,119,290 , GRCh37.p13 chr2: 183,950,500-183,984,018 DUSP19, NUP35
    nsv5195172mobile element insertion1nstd203human GRCh38 chr2: 183,145,001-183,145,018 , GRCh37.p13 chr2: 184,009,729-184,009,746 NUP35
    nsv5181666mobile element insertion1nstd203human GRCh38 chr2: 183,145,006-183,145,018 , GRCh37.p13 chr2: 184,009,734-184,009,746 NUP35
    nsv5180411mobile element insertion1nstd203human GRCh38 chr2: 183,116,592-183,116,605 , GRCh37.p13 chr2: 183,981,320-183,981,333 NUP35
    nsv5071705mobile element insertion1nstd203human GRCh38 chr2: 183,145,001-183,145,018 , GRCh37.p13 chr2: 184,009,729-184,009,746 NUP35
    nsv5033955inversion1nstd200human GRCh38 chr2: 103,800,446-187,202,765 , GRCh37.p13 chr2: 104,416,904-188,067,492 , EDDM3CP, 1184 more genes
    nsv4928956copy number variation1nstd200human GRCh38 chr2: 182,986,732-183,422,869 , GRCh37.p13 chr2: 183,851,460-184,287,597 , NUP35, 4 more genes
    nsv4916123copy number variation1nstd200human GRCh38 chr2: 183,156,494-183,173,979 , GRCh37.p13 chr2: 184,021,222-184,038,707 NUP35
    nsv4916122copy number variation1nstd200human GRCh38 chr2: 183,153,251-183,153,563 , GRCh37.p13 chr2: 184,017,979-184,018,291 NUP35
    nsv4916121copy number variation1nstd200human GRCh38 chr2: 183,124,918-183,125,473 , GRCh37.p13 chr2: 183,989,646-183,990,201 NUP35
    nsv4916120copy number variation1nstd200human GRCh38 chr2: 183,117,058-183,122,133 , GRCh37.p13 chr2: 183,981,786-183,986,861 NUP35
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