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Items: 1 to 20 of 206

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099257copy number variation1nstd231human GRCh38.p12 chr1: 203,396,218-207,103,915 , GRCh37 chr1: 203,365,346-207,277,260 ATP2B4, AVPR1B, 116 more genes
    nsv7095955copy number variation1nstd102humanUncertain significance GRCh37 chr1: 200,522,516-206,945,780 , GRCh38.p12 chr1: 200,553,388-206,772,435 ELF3, MAPKAPK2, 189 more genes
    nsv7095569copy number variation2nstd102humanUncertain significance GRCh37 chr1: 200,522,516-208,391,267 , GRCh38.p12 chr1: 200,553,388-208,217,922 TRK-TTT8-1, ADIPOR1, 228 more genes
    nsv7044734inversion1nstd229human GRCh38 chr1: 205,597,475-205,597,573 , GRCh37.p13 chr1: 205,566,603-205,566,701 MFSD4A
    nsv7044092inversion1nstd229human GRCh38 chr1: 203,118,726-211,305,271 , GRCh37.p13 chr1: 203,087,854-211,478,613 LOC100420418, LINC00260, 201 more genes
    nsv6671403copy number variation1nstd229human GRCh38 chr1: 205,582,728-205,587,186 , GRCh37.p13 chr1: 205,551,856-205,556,314 MFSD4A
    nsv6665467copy number variation1nstd229human GRCh38 chr1: 205,581,247-205,581,421 , GRCh37.p13 chr1: 205,550,375-205,550,549 MFSD4A
    nsv6636965copy number variation1nstd102humanPathogenic GRCh37 chr1: 181,453,460-213,107,248 , GRCh38.p12 chr1: 181,484,324-212,933,906 PRELP, SYT14, 527 more genes
    nsv6634372copy number variation1nstd102humanPathogenic GRCh37 chr1: 197,867,914-249,224,684 , GRCh38.p12 chr1: 197,898,784-248,930,485 LOC105373279, YBX1P9, 1036 more genes
    nsv6554773inversion1nstd223human GRCh38 chr1: 204,500,842-208,290,127 , GRCh37.p13 chr1: 204,469,970-208,463,472 RNA5SP75, LOC105372869, 108 more genes
    nsv6133967copy number variation1nstd213human GRCh37 chr1: 203,630,000-205,910,001 , GRCh38.p12 chr1: 203,660,872-205,940,873 PLEKHA6, KLHDC8A, 73 more genes
    nsv6133950copy number variation1nstd213human GRCh37 chr1: 178,070,000-205,920,001 , GRCh38.p12 chr1: 178,100,865-205,950,873 ADORA1, CACNA1E, 442 more genes
    nsv6133846copy number variation1nstd213human GRCh37 chr1: 203,140,000-205,920,001 , GRCh38.p12 chr1: 203,170,872-205,950,873 CHIT1, ELK4, 90 more genes
    nsv6133626copy number variation1nstd213human GRCh37 chr1: 205,160,000-206,320,001 , GRCh38.p12 chr1: 205,190,872-205,953,579 CDK18, LEMD1-AS1, 29 more genes
    nsv5449491copy number variation1nstd206human GRCh38 chr1: 205,600,693-205,602,139 , GRCh37.p13 chr1: 205,569,821-205,571,267 MFSD4A
    nsv5381285copy number variation2nstd102humanUncertain significance GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699 , DCST1, 2428 more genes
    nsv5078780mobile element insertion1nstd203human GRCh38 chr1: 205,593,418-205,593,421 , GRCh37.p13 chr1: 205,562,546-205,562,549 MFSD4A, RNU6-418P
    nsv5074596mobile element insertion1nstd203human GRCh38 chr1: 205,593,403-205,593,416 , GRCh37.p13 chr1: 205,562,531-205,562,544 MFSD4A, RNU6-418P
    nsv5073832mobile element insertion1nstd203human GRCh38 chr1: 205,593,416-205,593,418 , GRCh37.p13 chr1: 205,562,544-205,562,546 MFSD4A, RNU6-418P
    nsv5073635mobile element insertion1nstd203human GRCh38 chr1: 205,593,417-205,593,417 , GRCh37.p13 chr1: 205,562,545-205,562,545 MFSD4A, RNU6-418P
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