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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6634344copy number variation1nstd102humanPathogenic GRCh37 chrY: 2,650,140-9,651,417 , GRCh38.p12 chrY: 2,782,099-9,813,808 LOC105377235, TTTY7B, 135 more genes
    nsv6634094copy number variation4nstd224human GRCh37 chrY: 1-59,373,566 , GRCh38.p12 chrY: 10,001-57,217,415 ASMT, ASS1P6, 570 more genes
    nsv6315264copy number variation1nstd102humanPathogenic GRCh37 chrY: 2,650,140-7,114,097 , GRCh38.p12 chrY: 2,782,099-7,246,056 RNU6-1334P, SRIP3, 50 more genes
    nsv6315229copy number variation1nstd102humanPathogenic GRCh37 chrY: 1-59,373,566 , GRCh38.p12 chrY: 10,001-57,217,415 RBMY2VP, RFTN1P1, 570 more genes
    nsv6314745copy number variation1nstd102humanPathogenic GRCh37 chrY: 2,650,424-28,799,654 , GRCh38.p12 chrY: 2,782,383-26,653,507 TTTY20, USP9YP18, 524 more genes
    nsv6314504complex chromosomal rearrangement2nstd102humanLikely pathogenic GRCh38.p12 chrY: 5,024,484-5,024,484 , GRCh38.p12 chrY: 5,024,486-5,024,486 , GRCh37 chrY: 4,892,525-4,892,525 , GRCh37 chrY: 4,892,527-4,892,527 , GRCh37 chr3: 77,220,640-77,220,640 , GRCh37 chr3: 77,220,642-77,220,642 , GRCh38.p12 chr3: 77,171,489-77,171,489 , GRCh38.p12 chr3: 77,171,491-77,171,491 ROBO2, PCDH11Y
    nsv6294287copy number variation1nstd186human GRCh37 chrY: 5,473,429-5,479,429 , GRCh38.p12 chrY: 5,605,388-5,611,388 PCDH11Y
    nsv6290500copy number variation1nstd102humanLikely benign GRCh37 chrY: 3,037,425-5,670,611 , GRCh38.p12 chrY: 3,169,384-5,802,570 EIF4A1P2, RNU6-303P, 16 more genes
    nsv6243073mobile element insertion1nstd215human GRCh38 chrY: 5,449,061-5,449,061 , GRCh37.p13 chrY: 5,317,102-5,317,102 PCDH11Y
    nsv6138817copy number variation1nstd206human GRCh38 chrY: 5,605,388-5,611,388 , GRCh37.p13 chrY: 5,473,429-5,479,429 PCDH11Y
    nsv6138510copy number variation1nstd206human GRCh38 chrY: 5,361,888-5,376,488 , GRCh37.p13 chrY: 5,229,929-5,244,529 PCDH11Y
    nsv5978449copy number variation1nstd209human GRCh38 chrY: 5,101,759-5,107,532 , GRCh37.p13 chrY: 4,969,800-4,975,573 PCDH11Y
    nsv5977269copy number variation1nstd209human GRCh38 chrY: 5,357,348-5,373,374 , GRCh37.p13 chrY: 5,225,389-5,241,415 PCDH11Y
    nsv5972927copy number variation1nstd209human GRCh38 chrY: 5,101,394-5,112,367 , GRCh37.p13 chrY: 4,969,435-4,980,408 PCDH11Y
    nsv5723197mobile element insertion1nstd211human GRCh38 chrY: 5,027,408-5,027,408 , GRCh37.p13 chrY: 4,895,449-4,895,449 PCDH11Y
    nsv5671890copy number variation1nstd207human GRCh38 chrY: 5,348,007-5,348,076 , GRCh37.p13 chrY: 5,216,048-5,216,117 PCDH11Y
    nsv5671782inversion1nstd207human GRCh38 chrY: 10,002-57,217,414 , GRCh37.p13 chrY: 10,002-59,363,565 , ACTG1P2, 580 more genes
    nsv5671274copy number variation1nstd207human GRCh38 chrY: 5,092,130-5,092,179 , GRCh37.p13 chrY: 4,960,171-4,960,220 PCDH11Y
    nsv5669850copy number variation1nstd207human GRCh38 chrY: 5,311,482-5,311,535 , GRCh37.p13 chrY: 5,179,523-5,179,576 PCDH11Y
    nsv5669653copy number variation1nstd207human GRCh38 chrY: 5,107,772-5,108,097 , GRCh37.p13 chrY: 4,975,813-4,976,138 PCDH11Y
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