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Items: 1 to 20 of 1263

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv2661372copy number variation6estd199human GRCh37 chr12: 84,266,769-84,766,012 , GRCh38.p12 chr12: 83,872,990-84,372,233 LOC107984536
    esv2666739copy number variation325estd199human GRCh37 chr1: 207,699,545-207,737,892 , GRCh38.p12 chr1: 207,526,200-207,564,547 CR1
    esv2673583copy number variation519estd199human GRCh37 chr20: 1,560,991-1,594,041 , GRCh38.p12 chr20: 1,580,345-1,613,395 SIRPB1
    esv2666901copy number variation459estd199human GRCh37 chr11: 1,915,249-1,937,009 , GRCh38.p12 chr11: 1,894,019-1,915,779 LINC01150
    esv2675924copy number variation1estd199human GRCh37 chr13: 45,407,794-45,427,283 , GRCh38.p12 chr13: 44,833,658-44,853,147 LOC105370187
    esv2671922copy number variation12estd199human GRCh37 chr3: 89,531,431-89,547,075 , GRCh38.p12 chr3: 89,482,281-89,497,925 EPHA3
    esv2662901copy number variation324estd199human GRCh37 chr9: 41,969,445-41,984,392 , GRCh38.p12 chr9: 39,824,427-39,839,374 FGF7P3
    esv2676497copy number variation51estd199human GRCh37 chr4: 98,172,511-98,187,404 , GRCh38.p12 chr4: 97,251,360-97,266,253 STPG2
    esv2667088copy number variation20estd199human GRCh37 chr4: 98,172,511-98,187,404 , GRCh38.p12 chr4: 97,251,360-97,266,253 STPG2
    esv2657156copy number variation50estd199human GRCh37 chr21: 23,652,945-23,666,892 , GRCh38.p12 chr21: 22,280,625-22,294,572 , GRCh38.p12 chr21|NW_003315968.2: 184,854-198,801 LOC107985508
    esv2677364copy number variation34estd199human GRCh37 chr7: 91,029,645-91,042,742 , GRCh38.p12 chr7: 91,400,330-91,413,427 LINC02932
    esv2670787copy number variation158estd199human GRCh37 chr7: 151,134-160,557 , GRCh38.p12 chr7: 151,134-160,557 , GRCh38.p12 chr7|NT_187558.1: 106,939-119,904 , GRCh38.p12 chr7|NT_187653.1: 143,455-152,878 LINC03014
    esv2659442copy number variation87estd199human GRCh37 chr7: 150,945-159,992 , GRCh38.p12 chr7: 150,945-159,992 , GRCh38.p12 chr7|NT_187558.1: 106,750-119,335 , GRCh38.p12 chr7|NT_187653.1: 143,266-152,313 LINC03014
    esv2665944copy number variation17estd199human GRCh37 chr18: 14,449,245-14,461,392 , GRCh38.p12 chr18: 14,449,246-14,461,393 LONRF2P1
    esv2659639copy number variation40estd199human GRCh37 chr15: 76,883,945-76,895,542 , GRCh38.p12 chr15: 76,591,604-76,603,201 SCAPER
    esv2665606copy number variation90estd199human GRCh37 chr7: 91,031,083-91,042,584 , GRCh38.p12 chr7: 91,401,768-91,413,269 LINC02932
    esv2675519copy number variation112estd199human GRCh37 chr18: 66,745,594-66,756,999 , GRCh38.p12 chr18: 69,078,357-69,089,762 CCDC102B
    esv2659375copy number variation188estd199human GRCh37 chr21: 23,654,900-23,666,003 , GRCh38.p12 chr21: 22,282,580-22,293,683 , GRCh38.p12 chr21|NW_003315968.2: 186,809-197,912 LOC107985508
    esv2675250copy number variation1estd199human GRCh37 chr3: 98,140,844-98,151,628 , GRCh38.p12 chr3: 98,422,000-98,432,784 UBFD1P1
    esv2657233copy number variation3estd199human GRCh37 chr3: 195,133,675-195,144,429 , GRCh38.p12 chr3: 195,412,946-195,423,700 ACAP2
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