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Items: 1 to 20 of 309

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148056copy number variation1nstd102humanPathogenic GRCh37 chr2: 186,698,504-223,918,111 , GRCh38.p12 chr2: 185,833,777-223,053,393 DNAJB1P1, MTCO2P17, 580 more genes
    nsv7055370inversion1nstd229human GRCh38 chr2: 196,521,330-196,912,817 , GRCh37.p13 chr2: 197,386,054-197,777,541 CCDC150, PGAP1, 5 more genes
    nsv7045795inversion1nstd229human GRCh38 chr2: 195,566,013-199,490,438 , GRCh37.p13 chr2: 196,430,737-200,355,161 LINC01827, LOC107985972, 48 more genes
    nsv7044863inversion1nstd229human GRCh38 chr2: 196,869,008-196,870,501 , GRCh37.p13 chr2: 197,733,732-197,735,225 PGAP1
    nsv6697726copy number variation1nstd229human GRCh38 chr2: 196,752,641-197,291,148 , GRCh37.p13 chr2: 197,617,365-198,155,872 ANKRD44-AS1, GTF3C3, 7 more genes
    nsv6697182copy number variation1nstd229human GRCh38 chr2: 192,562,889-202,434,958 , GRCh37.p13 chr2: 193,427,615-203,299,681 RNU6-915P, SLC44A3P1, 150 more genes
    nsv6691904copy number variation1nstd229human GRCh38 chr2: 196,828,236-196,833,784 , GRCh37.p13 chr2: 197,692,960-197,698,508 PGAP1
    nsv6687557copy number variation1nstd229human GRCh38 chr2: 196,865,940-196,873,012 , GRCh37.p13 chr2: 197,730,664-197,737,736 PGAP1
    nsv6686927copy number variation1nstd229human GRCh38 chr2: 196,868,419-196,868,765 , GRCh37.p13 chr2: 197,733,143-197,733,489 PGAP1
    nsv6686516copy number variation1nstd229human GRCh38 chr2: 196,868,919-196,869,768 , GRCh37.p13 chr2: 197,733,643-197,734,492 PGAP1
    nsv6685718copy number variation1nstd229human GRCh38 chr2: 196,830,093-196,838,452 , GRCh37.p13 chr2: 197,694,817-197,703,176 PGAP1
    nsv6684982copy number variation1nstd229human GRCh38 chr2: 196,899,611-196,900,270 , GRCh37.p13 chr2: 197,764,335-197,764,994 PGAP1
    nsv6682364copy number variation1nstd229human GRCh38 chr2: 196,872,903-196,936,680 , GRCh37.p13 chr2: 197,737,627-197,801,404 PGAP1
    nsv6637127copy number variation1nstd102humanPathogenic GRCh37 chr2: 189,909,904-209,468,383 , GRCh38.p12 chr2: 189,045,178-208,603,658 LOC100421409, LOC100507443, 310 more genes
    nsv6636947copy number variation1nstd102humanUncertain significance GRCh37 chr2: 197,704,153-198,552,092 , GRCh38.p12 chr2: 196,839,429-197,687,368 SF3B1, RPL4P7, 17 more genes
    nsv6636571copy number variation1nstd102humanPathogenic GRCh37 chr2: 187,152,754-199,960,525 , GRCh38.p12 chr2: 186,288,027-199,095,802 GAPDHP59, OSGEPL1-AS1, 135 more genes
    nsv6548994inversion1nstd223human GRCh38 chr2: 196,914,542-196,914,956 , GRCh37.p13 chr2: 197,779,266-197,779,680 PGAP1
    nsv6548929inversion1nstd223human GRCh38 chr2: 196,889,638-196,890,225 , GRCh37.p13 chr2: 197,754,362-197,754,949 PGAP1
    nsv6542672inversion1nstd223human GRCh38 chr2: 196,886,972-196,887,139 , GRCh37.p13 chr2: 197,751,696-197,751,863 PGAP1
    nsv6541949inversion1nstd223human GRCh38 chr2: 196,832,074-196,832,630 , GRCh37.p13 chr2: 197,696,798-197,697,354 PGAP1
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