U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Search results

Items: 1 to 20 of 45

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4360640inversion1nstd169human GRCh38.p12 chr6: 141,866,324-141,898,714 , GRCh37.p13 chr6: 142,187,461-142,219,851 LOC105378031
    nsv4360625inversion1nstd169human GRCh37.p13 chrX: 75,361,703-75,373,076 , GRCh38.p12 chrX: 76,141,868-76,153,241
    nsv4360639inversion1nstd169human GRCh38.p12 chr6: 106,720,678-106,723,661 , GRCh37.p13 chr6: 107,168,553-107,171,536 LINC02532
    nsv4360655inversion1nstd169human GRCh38.p12 chr4: 40,233,407-40,235,440 , GRCh37.p13 chr4: 40,235,027-40,237,060 RHOH
    nsv4360612inversion1nstd169human GRCh38.p12 chr1: 187,495,697-187,497,600 , GRCh37.p13 chr1: 187,464,829-187,466,732 LOC105371656
    nsv4360646inversion1nstd169human GRCh37.p13 chr5: 147,553,040-147,554,778 , GRCh38.p12 chr5: 148,173,477-148,175,215 SPINK14
    nsv4360652inversion1nstd169human GRCh37.p13 chr3: 41,362,143-41,363,805 , GRCh38.p12 chr3: 41,320,652-41,322,314 ULK4
    nsv4360622inversion1nstd169human GRCh37.p13 chrX: 6,137,047-6,138,392 , GRCh38.p12 chrX: 6,219,006-6,220,351 NLGN4X
    nsv4360641inversion1nstd169human GRCh37.p13 chr7: 40,879,375-40,880,470 , GRCh38.p12 chr7: 40,839,776-40,840,871 SUGCT
    nsv4360629inversion1nstd169human GRCh38.p12 chr16: 85,155,108-85,156,198 , GRCh37.p13 chr16: 85,188,714-85,189,804 LOC105371382
    nsv4360650inversion1nstd169human GRCh38.p12 chr6: 89,213,909-89,214,232 , GRCh37.p13 chr6: 89,923,628-89,923,951 GABRR1
    nsv4360614inversion1nstd169human GRCh38.p12 chr1: 205,209,479-205,209,706 , GRCh37.p13 chr1: 205,178,607-205,178,834 DSTYK
    nsv4360626inversion1nstd169human GRCh37.p13 chrX: 100,852,522-100,871,235 , GRCh38.p12 chrX: 101,597,544-101,616,245 ARMCX6, ARMCX7P
    nsv4360628inversion1nstd169human GRCh37.p13 chr16: 75,239,540-75,257,217 , GRCh38.p12 chr16: 75,205,642-75,223,319 CTRB1, CTRB2
    nsv4360644inversion1nstd169human GRCh37.p13 chr9: 115,867,543-115,881,590 , GRCh38.p12 chr9: 113,105,263-113,119,310 FAM225A, FAM225B
    nsv4360634inversion1nstd169human GRCh37.p13 chr11: 310,225-319,555 , GRCh38.p12 chr11: 310,225-319,555 IFITM1, IFITM3
    nsv4360624inversion1nstd169human GRCh37.p13 chrX: 72,215,927-72,306,774 , GRCh38.p12 chrX: 72,996,088-73,086,935 PABPC1L2A, PABPC1L2B, 2 more genes
    nsv4360619inversion1nstd169human GRCh37.p13 chrX: 153,566,408-153,622,435 , GRCh38.p12 chrX: 154,338,058-154,394,093 EMD, FLNA, 1 more genes
    nsv4360636inversion1nstd169human GRCh37.p13 chr13: 64,290,984-64,343,590 , GRCh38.p12 chr13: 63,716,851-63,769,457 OR7E156P, LINC00395, 2 more genes
    nsv4360651inversion1nstd169human GRCh37.p13 chr2: 241,615,561-241,638,174 , GRCh38.p12 chr2: 240,676,144-240,698,757 LOC285191, AQP12A, 1 more genes
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Search details

    See more...

    Recent activity

    Clear Turn Off Turn On

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

    See more...
    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
    Support Center