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Items: 1 to 20 of 193

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148054copy number variation1nstd102humanPathogenic GRCh37 chr1: 142,535,935-157,648,813 , GRCh38.p12 chr1: 120,175,847-149,601,750 , TRN-GTT12-1, 266 more genes
    nsv7098724copy number variation1nstd102humanPathogenic GRCh37 chr1: 146,397,357-148,344,744 , GRCh38.p12 chr1: 144,536,526-148,549,211 , LOC105371217, 150 more genes
    nsv7056211inversion1nstd229human GRCh38 chr1: 143,881,700-152,159,818 , GRCh37.p13 chr1|NW_003871055.3: 697,113-7,283,150 , PDIA3P1, 333 more genes
    nsv7045394inversion1nstd229human GRCh38 chr1: 143,732,174-147,339,264 , GRCh37.p13 chr1|NW_003871055.3: 547,587-4,154,677 , MIR6736, 130 more genes
    nsv7045117inversion1nstd229human GRCh38 chr1: 143,671,956-145,963,983 , GRCh37.p13 chr1|NW_003871055.3: 487,369-2,779,396 , GPR89A, 96 more genes
    nsv6634349copy number variation1nstd102humanPathogenic GRCh37 chr1: 145,157,447-148,016,122 , GRCh38.p12 chr1: 144,536,526-149,492,442 , TRN-GTT10-1, 170 more genes
    nsv6546879inversion1nstd223human GRCh38 chr1: 144,076,969-144,882,593 , GRCh37.p13 chr1|NW_003871055.3: 892,382-1,698,006 PPIAL4F, LINC01632, 28 more genes
    nsv6537837inversion1nstd223human GRCh38 chr1: 144,077,928-144,882,652 , GRCh37.p13 chr1|NW_003871055.3: 893,341-1,698,065 NBPF15, LOC100996731, 28 more genes
    nsv6536769inversion1nstd223human GRCh38 chr1: 144,077,918-144,883,948 , GRCh37.p13 chr1|NW_003871055.3: 893,331-1,699,361 RNA5SP59, LOC105371217, 28 more genes
    nsv6290404copy number variation1nstd102humanPathogenic GRCh37 chr1: 146,043,714-148,514,899 , GRCh38.p12 chr1: 144,536,526-148,549,211 , TRN-GTT9-2, 150 more genes
    nsv6290073copy number variation1nstd218human GRCh38.p12 chr1: 143,511,409-149,082,254 , GRCh37 chr1: 147,824,148-149,378,266 , BCL9, 215 more genes
    nsv6290071copy number variation1nstd218human GRCh38.p12 chr1: 143,511,409-149,082,254 , GRCh37 chr1: 147,806,599-149,209,289 , BCL9, 215 more genes
    nsv6138264copy number variation1nstd206human GRCh38 chr1: 144,712,000-144,718,587 , GRCh37.p13 chr1|NW_003871055.3: 1,527,413-1,534,000 LSP1P5
    nsv6107885inversion1nstd212human GRCh37.p13 chr1|NW_003871055.3: 1,368,352-3,822,544 , GRCh38 chr1: 144,552,939-147,007,131 , DRD5P2, 85 more genes
    nsv5977192inversion1nstd209human GRCh37.p13 chr1|NW_003871055.3: 892,357-1,698,998 , GRCh38 chr1: 144,076,944-144,883,585 , DRD5P2, 32 more genes
    nsv5885134copy number variation1nstd209human GRCh38 chr1: 143,707,729-148,368,205 , GRCh37.p13 chr1|NW_003871055.3: 523,142-5,183,618 , TRN-GTT22-1, 183 more genes
    nsv5425440copy number variation1nstd206human GRCh38 chr1: 144,142,587-144,832,587 , GRCh37.p13 chr1|NW_003871055.3: 958,000-1,648,000 , LOC105371216, 29 more genes
    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
    nsv5211424copy number variation1nstd204human GRCh38.p13 chr1: 144,735,501-144,736,500 , GRCh37.p13 chr1|NW_003871055.3: 1,550,914-1,551,913 LSP1P5
    nsv5209204copy number variation1nstd204human GRCh38.p13 chr1: 144,734,001-144,779,100 , GRCh37.p13 chr1|NW_003871055.3: 1,549,414-1,594,513 LSP1P5, LOC100996737
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