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Items: 1 to 20 of 101

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7053998inversion1nstd229human GRCh38 chr5: 148,749,982-154,424,819 , GRCh37.p13 chr5: 148,129,545-153,804,379 HMGXB3, RN7SL868P, 102 more genes
    nsv7040531inversion1nstd229human GRCh38 chr5: 151,482,879-155,518,141 , GRCh37.p13 chr5: 150,862,440-154,897,701 RN7SL803P, MRPL22, 56 more genes
    nsv6795609copy number variation1nstd229human GRCh38 chr5: 154,039,601-154,047,900 , GRCh37.p13 chr5: 153,419,161-153,427,460 MFAP3
    nsv6789292copy number variation1nstd229human GRCh38 chr5: 153,762,366-154,230,388 , GRCh37.p13 chr5: 153,141,926-153,609,948 MFAP3, GRIA1, 6 more genes
    nsv6780836copy number variation1nstd229human GRCh38 chr5: 154,035,262-154,037,842 , GRCh37.p13 chr5: 153,414,822-153,417,402 FAM114A2, MFAP3
    nsv6779255copy number variation1nstd229human GRCh38 chr5: 154,033,710-154,039,091 , GRCh37.p13 chr5: 153,413,270-153,418,651 FAM114A2, MFAP3
    nsv6779247copy number variation1nstd229human GRCh38 chr5: 153,995,694-154,050,116 , GRCh37.p13 chr5: 153,375,254-153,429,676 MFAP3, FAM114A2
    nsv6637008copy number variation1nstd102humanUncertain significance GRCh37 chr5: 153,030,768-153,594,725 , GRCh38.p12 chr5: 153,651,208-154,215,165 MFAP3, GALNT10, 6 more genes
    nsv6636891copy number variation1nstd102humanPathogenic GRCh37 chr5: 150,535,183-172,906,793 , GRCh38.p12 chr5: 151,155,622-173,479,790 EFCAB9, LOC112267936, 287 more genes
    nsv6315448copy number variation1nstd102humanPathogenic GRCh37 chr5: 149,010,383-180,719,789 , GRCh38.p12 chr5: 149,630,820-181,292,788 GRM6, MIR1229, 554 more genes
    nsv6135389copy number variation1nstd213human GRCh37 chr5: 153,260,000-153,420,001 , GRCh38.p12 chr5: 153,880,440-154,040,441 MFAP3, FAM114A2, 3 more genes
    nsv6135388copy number variation1nstd213human GRCh37 chr5: 153,010,000-160,030,001 , GRCh38.p12 chr5: 153,630,440-160,602,994 ADRA1B, EBF1, 107 more genes
    nsv6135205copy number variation1nstd213human GRCh37 chr5: 91,690,000-180,740,001 , GRCh38.p12 chr5: 92,354,293-181,313,000 ADRA1B, ASS1P10, 1378 more genes
    nsv5563339inversion1nstd206human GRCh38 chr5: 154,047,107-154,049,675 , GRCh37.p13 chr5: 153,426,667-153,429,235 MFAP3
    nsv5545531insertion1nstd206human GRCh38 chr5: 154,047,150-154,047,162 , GRCh37.p13 chr5: 153,426,710-153,426,722 MFAP3
    nsv5459047copy number variation1nstd206human GRCh38 chr5: 154,047,712-154,048,473 , GRCh37.p13 chr5: 153,427,272-153,428,033 MFAP3
    nsv5080438mobile element insertion1nstd203human GRCh38 chr5: 154,047,121-154,047,130 , GRCh37.p13 chr5: 153,426,681-153,426,690 MFAP3
    nsv5036421inversion1nstd200human GRCh38 chr5: 85,193,812-162,906,830 , GRCh37.p13 chr5: 84,489,630-162,333,836 , PRR16, 1116 more genes
    nsv4947215copy number variation1nstd200human GRCh38 chr5: 93,957,557-155,223,076 , GRCh37.p13 chr5: 93,293,262-154,602,636 , TGFBI, 937 more genes
    nsv4939315copy number variation1nstd200human GRCh38 chr5: 154,054,272-154,059,905 , GRCh37.p13 chr5: 153,433,832-153,439,465 MFAP3
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