ClinVar Miner

List of variants in gene INVS reported as uncertain significance for abdominal and pelvic region disorder

Included ClinVar conditions (961):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 106
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HGVS dbSNP
NC_000009.12:g.(?_100226042)_(100226255_?)del
NM_014425.5(INVS):c.*158T>C
NM_014425.5(INVS):c.*323A>T
NM_014425.5(INVS):c.*352A>T
NM_014425.5(INVS):c.*415A>G
NM_014425.5(INVS):c.*45G>A
NM_014425.5(INVS):c.*466_*467CA[18] rs10527613
NM_014425.5(INVS):c.*466_*467CA[19] rs10527613
NM_014425.5(INVS):c.*466_*467CA[21] rs10527613
NM_014425.5(INVS):c.*466_*467CA[23] rs10527613
NM_014425.5(INVS):c.*466_*467insTCAC rs200314659
NM_014425.5(INVS):c.*466_*467insTCACAC rs200314659
NM_014425.5(INVS):c.*467A>T
NM_014425.5(INVS):c.*469A>T rs886063279
NM_014425.5(INVS):c.*5C>T
NM_014425.5(INVS):c.*73T>A rs886063273
NM_014425.5(INVS):c.*98A>G rs886063274
NM_014425.5(INVS):c.-129C>A rs533889420
NM_014425.5(INVS):c.-176C>T
NM_014425.5(INVS):c.-178G>A rs886063263
NM_014425.5(INVS):c.1056G>C (p.Met352Ile)
NM_014425.5(INVS):c.106+6C>T
NM_014425.5(INVS):c.1111A>G (p.Ser371Gly) rs200546215
NM_014425.5(INVS):c.118C>G (p.Leu40Val) rs148219510
NM_014425.5(INVS):c.1220A>C (p.Gln407Pro)
NM_014425.5(INVS):c.1256T>C (p.Val419Ala)
NM_014425.5(INVS):c.1264G>C (p.Asp422His)
NM_014425.5(INVS):c.1317C>T (p.Cys439=) rs886063266
NM_014425.5(INVS):c.1374C>A (p.Thr458=)
NM_014425.5(INVS):c.1379T>G (p.Leu460Trp) rs878854980
NM_014425.5(INVS):c.1396G>A (p.Gly466Arg) rs1554726564
NM_014425.5(INVS):c.1436A>G (p.Asn479Ser)
NM_014425.5(INVS):c.1459A>C (p.Lys487Gln) rs398124271
NM_014425.5(INVS):c.1464+1G>A rs375753623
NM_014425.5(INVS):c.1466G>A (p.Gly489Glu) rs1015507237
NM_014425.5(INVS):c.1490G>A (p.Cys497Tyr) rs1296545586
NM_014425.5(INVS):c.1571+2dup rs1554728033
NM_014425.5(INVS):c.1572A>G (p.Arg524=)
NM_014425.5(INVS):c.1606C>T (p.Arg536Cys)
NM_014425.5(INVS):c.1661T>C (p.Ile554Thr) rs748753412
NM_014425.5(INVS):c.166G>A (p.Val56Met)
NM_014425.5(INVS):c.1670T>G (p.Ile557Ser)
NM_014425.5(INVS):c.1675G>A (p.Ala559Thr)
NM_014425.5(INVS):c.1808G>A (p.Arg603Gln)
NM_014425.5(INVS):c.1899_1901CAG[1] (p.Ser634del) rs886063267
NM_014425.5(INVS):c.1913G>A (p.Arg638Gln) rs761806481
NM_014425.5(INVS):c.1916C>A (p.Ala639Asp) rs886063268
NM_014425.5(INVS):c.1943A>G (p.Asn648Ser) rs116686341
NM_014425.5(INVS):c.1945G>A (p.Val649Met) rs115042730
NM_014425.5(INVS):c.1971C>G (p.Asp657Glu) rs114942117
NM_014425.5(INVS):c.1976G>A (p.Arg659Lys)
NM_014425.5(INVS):c.2001C>T (p.Gly667=) rs536554704
NM_014425.5(INVS):c.2009T>C (p.Leu670Pro) rs762112247
NM_014425.5(INVS):c.2021A>G (p.Gln674Arg)
NM_014425.5(INVS):c.2056A>G (p.Arg686Gly) rs150001738
NM_014425.5(INVS):c.2108T>C (p.Val703Ala)
NM_014425.5(INVS):c.2152G>C (p.Gly718Arg) rs1554730698
NM_014425.5(INVS):c.2200C>T (p.Arg734Trp) rs370949695
NM_014425.5(INVS):c.2210A>G (p.Lys737Arg)
NM_014425.5(INVS):c.2232G>C (p.Gln744His)
NM_014425.5(INVS):c.2260G>A (p.Asp754Asn) rs115401137
NM_014425.5(INVS):c.2278T>G (p.Ser760Ala) rs146901872
NM_014425.5(INVS):c.2279C>T (p.Ser760Phe)
NM_014425.5(INVS):c.2285G>A (p.Arg762Gln)
NM_014425.5(INVS):c.2310C>T (p.His770=) rs116606949
NM_014425.5(INVS):c.2335C>T (p.Arg779Trp) rs370643191
NM_014425.5(INVS):c.2380C>T (p.Arg794Cys) rs556807161
NM_014425.5(INVS):c.2381G>A (p.Arg794His)
NM_014425.5(INVS):c.2386C>G (p.Gln796Glu) rs147731667
NM_014425.5(INVS):c.2417C>T (p.Ala806Val)
NM_014425.5(INVS):c.2428C>T (p.Arg810Cys) rs984016152
NM_014425.5(INVS):c.2441C>T (p.Ala814Val) rs886063269
NM_014425.5(INVS):c.2443C>T (p.Arg815Trp) rs564509196
NM_014425.5(INVS):c.2453C>T (p.Ala818Val) rs115324411
NM_014425.5(INVS):c.2454G>A (p.Ala818=) rs115937161
NM_014425.5(INVS):c.2489C>T (p.Thr830Ile) rs886063270
NM_014425.5(INVS):c.2520C>T (p.Leu840=)
NM_014425.5(INVS):c.2570C>T (p.Ser857Leu)
NM_014425.5(INVS):c.2686G>A (p.Val896Ile) rs114847355
NM_014425.5(INVS):c.2714G>A (p.Arg905Lys)
NM_014425.5(INVS):c.2764G>C (p.Val922Leu)
NM_014425.5(INVS):c.2776G>A (p.Ala926Thr) rs374891838
NM_014425.5(INVS):c.2782C>T (p.Arg928Ter) rs376879175
NM_014425.5(INVS):c.2783G>A (p.Arg928Gln)
NM_014425.5(INVS):c.2785A>G (p.Ser929Gly) rs116188920
NM_014425.5(INVS):c.2803C>T (p.His935Tyr) rs139768159
NM_014425.5(INVS):c.2819G>A (p.Arg940Gln) rs369751285
NM_014425.5(INVS):c.284G>A (p.Arg95His) rs372088206
NM_014425.5(INVS):c.286T>C (p.Phe96Leu)
NM_014425.5(INVS):c.2874A>G (p.Thr958=) rs886063271
NM_014425.5(INVS):c.3028G>A (p.Glu1010Lys) rs375774619
NM_014425.5(INVS):c.3056C>G (p.Ser1019Cys) rs886063272
NM_014425.5(INVS):c.3099C>T (p.Asn1033=) rs368303175
NM_014425.5(INVS):c.3106T>C (p.Cys1036Arg)
NM_014425.5(INVS):c.433C>A (p.Gln145Lys)
NM_014425.5(INVS):c.501G>A (p.Leu167=)
NM_014425.5(INVS):c.564G>A (p.Trp188Ter) rs1564167474
NM_014425.5(INVS):c.67G>A (p.Val23Ile) rs145303373
NM_014425.5(INVS):c.67G>C (p.Val23Leu)
NM_014425.5(INVS):c.775C>T (p.Leu259=) rs886063264
NM_014425.5(INVS):c.796+4C>T rs371310920
NM_014425.5(INVS):c.889G>A (p.Ala297Thr) rs116475199
NM_014425.5(INVS):c.907-13dup rs750082874
NM_014425.5(INVS):c.907-7C>G
NM_014425.5(INVS):c.916A>G (p.Lys306Glu) rs878854981
NM_014425.5(INVS):c.962A>G (p.Glu321Gly)

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