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Items: 1 to 20 of 235

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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
    nsv7098849copy number variation1nstd102humanPathogenic GRCh37 chr3: 110,943,783-115,859,912 , GRCh38.p12 chr3: 111,224,936-116,141,065 ATG3, SIDT1, 81 more genes
    nsv7051524inversion1nstd229human GRCh38 chr3: 110,492,556-118,654,181 , GRCh37.p13 chr3: 110,211,403-118,373,028 MIR8076, ZBTB20-AS4, 106 more genes
    nsv7046343inversion1nstd229human GRCh38 chr3: 108,261,187-113,011,016 , GRCh37.p13 chr3: 107,980,034-112,729,863 LOC105374041, DIMT1P1, 69 more genes
    nsv7039416inversion1nstd229human GRCh38 chr3: 111,765,090-113,399,244 , GRCh37.p13 chr3: 111,483,937-113,118,091 SLC9C1, TAGLN3, 35 more genes
    nsv6715250copy number variation1nstd229human GRCh38 chr3: 112,588,076-112,600,241 , GRCh37.p13 chr3: 112,306,923-112,319,088 CCDC80
    nsv6713694copy number variation1nstd229human GRCh38 chr3: 112,586,249-112,779,718 , GRCh37.p13 chr3: 112,305,096-112,498,565 MIR9900, MAT2AP1, 2 more genes
    nsv6712007copy number variation1nstd229human GRCh38 chr3: 112,619,107-112,638,028 , GRCh37.p13 chr3: 112,337,954-112,356,875 CCDC80
    nsv6709607copy number variation1nstd229human GRCh38 chr3: 112,589,403-112,602,474 , GRCh37.p13 chr3: 112,308,250-112,321,321 CCDC80
    nsv6708836copy number variation1nstd229human GRCh38 chr3: 112,500,165-112,636,656 , GRCh37.p13 chr3: 112,219,012-112,355,503 ATG3, CCDC80, 3 more genes
    nsv6708743copy number variation1nstd229human GRCh38 chr3: 112,637,975-112,654,902 , GRCh37.p13 chr3: 112,356,822-112,373,749 CCDC80
    nsv6703604copy number variation1nstd229human GRCh38 chr3: 112,596,424-112,602,401 , GRCh37.p13 chr3: 112,315,271-112,321,248 CCDC80
    nsv6701576copy number variation1nstd229human GRCh38 chr3: 109,882,767-113,954,905 , GRCh37.p13 chr3: 109,601,614-113,673,752 SLC9C1, NECTIN3, 64 more genes
    nsv6636830copy number variation1nstd102humanPathogenic GRCh37 chr3: 107,059,705-115,005,256 , GRCh38.p12 chr3: 107,340,858-115,286,409 ATP6V1A, DRD3, 117 more genes
    nsv6636802copy number variation1nstd102humanUncertain significance GRCh37 chr3: 111,919,475-112,389,338 , GRCh38.p12 chr3: 112,200,628-112,670,491 LOC100532749, OR7E100P, 8 more genes
    nsv6628259copy number variation1nstd224human GRCh37 chr3: 112,324,305-112,497,880 , GRCh38.p12 chr3: 112,605,458-112,779,033 MIR9900, CCDC80, 2 more genes
    nsv6356406copy number variation1nstd223human GRCh38 chr3: 112,628,160-112,628,928 , GRCh37.p13 chr3: 112,347,007-112,347,775 CCDC80
    nsv6315408copy number variation1nstd102humanPathogenic GRCh37 chr3: 106,598,767-115,704,696 , GRCh38.p12 chr3: 106,879,920-115,985,849 DZIP3, MIR9900, 138 more genes
    nsv6134776copy number variation1nstd213human GRCh37 chr3: 105,120,000-116,510,001 , GRCh38.p12 chr3: 105,401,156-116,791,154 , ALCAM, 156 more genes
    nsv5723765mobile element insertion1nstd211human GRCh38 chr3: 112,604,991-112,604,991 , GRCh37.p13 chr3: 112,323,838-112,323,838 CCDC80
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