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Items: 1 to 20 of 269

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137157inversion1nstd234human GRCh37 chrX: 31,626,542-82,320,140 , GRCh38.p12 chrX: 31,608,425-83,065,132 ABCB7, ACTG1P10, 775 more genes
    nsv7137063copy number variation1nstd102humanPathogenic GRCh37 chrX: 200,855-155,240,074 , GRCh38.p12 chrX: 284,188-156,010,409 RN7SL581P, HMGB1P32, 2151 more genes
    nsv7088933copy number variation1nstd229human GRCh38 chrX: 75,724,001-75,779,500 , GRCh37.p13 chrX: 74,943,836-74,999,335 TTC3P1, LOC107985664
    nsv7088931copy number variation1nstd229human GRCh38 chrX: 75,714,401-75,779,500 , GRCh37.p13 chrX: 74,934,236-74,999,335 TTC3P1, LOC107985664
    nsv7088926copy number variation1nstd229human GRCh38 chrX: 75,677,512-76,120,400 , GRCh37.p13 chrX: 74,897,347-75,200,415 ARL5AP5, MAGEE2, 3 more genes
    nsv7088921copy number variation1nstd229human GRCh38 chrX: 75,620,051-76,168,081 , GRCh37.p13 chrX: 74,839,886-75,200,415 ARL5AP5, MAGEE2, 3 more genes
    nsv7027122inversion1nstd229human GRCh38 chrX: 74,878,735-76,069,015 , GRCh37.p13 chrX: 74,098,570-75,200,415 TERF1P7, ZDHHC15, 13 more genes
    nsv7021765inversion1nstd229human GRCh38 chrX: 75,723,584-75,779,486 , GRCh37.p13 chrX: 74,943,419-74,999,321 TTC3P1, LOC107985664
    nsv6636397copy number variation1nstd102humanUncertain significance GRCh37 chrX: 74,938,239-75,361,671 , GRCh38.p12 chrX: 75,718,404-76,141,836 LOC107985664, MAGEE2, 3 more genes
    nsv6636208copy number variation1nstd102humanUncertain significance GRCh37 chrX: 74,946,710-76,904,755 , GRCh38.p12 chrX: 75,726,875-77,649,265 FGF16, SPRYD7P1, 19 more genes
    nsv6634242copy number variation1nstd224human GRCh37 chrX: 1-155,270,560 , GRCh38.p12 chrX: 10,001-156,030,895 NR0B1, ALAS2, 2154 more genes
    nsv6315393copy number variation1nstd102humanPathogenic GRCh37 chrX: 61,545-155,226,048 , GRCh38.p12 chrX: 11,545-155,996,383 H2BP8, LOC101060199, 2151 more genes
    nsv6315389copy number variation1nstd102humanPathogenic GRCh37 chrX: 11,522,765-155,233,731 , GRCh38.p12 chrX: 11,504,645-156,004,066 RBMX, LOC100129144, 2042 more genes
    nsv6315332copy number variation1nstd102humanPathogenic GRCh37 chrX: 62,685,885-155,233,731 , GRCh38.p12 chrX: 63,466,005-156,004,066 MAGT1, TAFAZZIN, 1337 more genes
    nsv6315331copy number variation4nstd102humanPathogenic GRCh37 chrX: 1-155,270,560 , GRCh38.p12 chrX: 10,001-156,030,895 PLAC1, PGK1P1, 2154 more genes
    nsv6313464copy number variation1nstd102humanUncertain significance GRCh37 chrX: 72,095,006-88,455,505 , GRCh38.p12 chrX: 72,875,172-89,200,506 LOC105373285, LOC105373288, 170 more genes
    nsv6313346copy number variation1nstd102humanPathogenic GRCh37 chrX: 61,974,855-79,123,671 , GRCh38.p12 chrX: 62,755,385-79,868,171 RPS7P14, RNY4P23, 280 more genes
    nsv6313230copy number variation1nstd102humanPathogenic GRCh37 chrX: 61,877,278-79,123,671 , GRCh38.p12 chrX: 62,657,808-79,868,171 SSBL2P, LOC105373239, 280 more genes
    nsv6137629copy number variation1nstd213human GRCh37 chrX: 66,030,000-152,230,001 , GRCh38.p12 chrX: 66,810,158-153,061,271 ABCB7, AGTR2, 1162 more genes
    nsv6137410copy number variation1nstd213human GRCh37 chrX: 73,930,000-75,350,001 , GRCh38.p12 chrX: 74,710,165-76,130,166 ABCB7, UPRT, 13 more genes
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