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Items: 1 to 20 of 269

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148201copy number variation1nstd102humanPathogenic GRCh38 chr3: 93,979,547-124,774,010 , GRCh37.p13 chr3: 93,698,391-124,492,857 NECTIN3, H2BP3, 418 more genes
    nsv7096531copy number variation1nstd102humanUncertain significance GRCh37 chr3: 121,489,192-125,313,644 , GRCh38.p12 chr3: 121,770,345-125,594,800 MEMO1P6, HACD2, 62 more genes
    nsv7049846inversion1nstd229human GRCh38 chr3: 122,823,462-122,823,490 , GRCh37.p13 chr3: 122,542,309-122,542,337 SLC49A4
    nsv6717928copy number variation1nstd229human GRCh38 chr3: 122,561,318-123,338,455 , GRCh37.p13 chr3: 122,280,165-123,057,302 PARP15, HSPBAP1, 12 more genes
    nsv6713021copy number variation1nstd229human GRCh38 chr3: 122,812,801-122,815,800 , GRCh37.p13 chr3: 122,531,648-122,534,647 SLC49A4
    nsv6712664copy number variation1nstd229human GRCh38 chr3: 122,829,501-122,840,000 , GRCh37.p13 chr3: 122,548,348-122,558,847 SLC49A4
    nsv6708846copy number variation1nstd229human GRCh38 chr3: 122,888,401-122,892,900 , GRCh37.p13 chr3: 122,607,248-122,611,747 LINC02035, SLC49A4
    nsv6708315copy number variation1nstd229human GRCh38 chr3: 122,853,374-122,853,443 , GRCh37.p13 chr3: 122,572,221-122,572,290 SLC49A4
    nsv6707858copy number variation1nstd229human GRCh38 chr3: 122,755,415-122,835,916 , GRCh37.p13 chr3: 122,474,262-122,554,763 HSPBAP1, SLC49A4
    nsv6703931copy number variation1nstd229human GRCh38 chr3: 118,573,267-126,079,281 , GRCh37.p13 chr3: 118,292,114-125,798,124 RPS24P9, LOC105374064, 149 more genes
    nsv6701071copy number variation1nstd229human GRCh38 chr3: 122,885,006-122,885,225 , GRCh37.p13 chr3: 122,603,853-122,604,072 LINC02035, SLC49A4
    nsv6699440copy number variation1nstd229human GRCh38 chr3: 122,799,437-122,799,974 , GRCh37.p13 chr3: 122,518,284-122,518,821 SLC49A4
    nsv6637156copy number variation1nstd102humanPathogenic GRCh37 chr3: 116,620,308-172,042,292 , GRCh38.p12 chr3: 116,901,461-172,324,502 H1-10, AADACL2-AS1, 846 more genes
    nsv6628684copy number variation1nstd224human GRCh37 chr3: 122,418,238-122,689,412 , GRCh38.p12 chr3: 122,699,391-122,970,565 PARP14, SLC49A4, 3 more genes
    nsv6628267copy number variation1nstd224human GRCh37 chr3: 122,478,673-122,630,323 , GRCh38.p12 chr3: 122,759,826-122,911,476 SLC49A4, LINC02035, 2 more genes
    nsv6628205copy number variation1nstd224human GRCh37 chr3: 122,479,371-122,632,248 , GRCh38.p12 chr3: 122,760,524-122,913,401 SEMA5B, SLC49A4, 2 more genes
    nsv6628204copy number variation1nstd224human GRCh37 chr3: 122,461,416-122,518,334 , GRCh38.p12 chr3: 122,742,569-122,799,487 HSPBAP1, SLC49A4
    nsv6568609inversion1nstd223human GRCh38 chr3: 122,852,126-122,853,757 , GRCh37.p13 chr3: 122,570,973-122,572,604 SLC49A4
    nsv6374903copy number variation1nstd223human GRCh38 chr3: 122,772,001-122,801,600 , GRCh37.p13 chr3: 122,490,848-122,520,447 HSPBAP1, SLC49A4
    nsv6373863copy number variation1nstd223human GRCh38 chr3: 122,780,601-122,804,000 , GRCh37.p13 chr3: 122,499,448-122,522,847 SLC49A4, HSPBAP1
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